Reviews Zantac Injection


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Zantac Injection Drug Description
ZANTAC®
(ranitidine hydrochloride) Injection
ZANTAC®
(ranitidine hydrochloride) Injection Premixed
DRUG DESCRIPTION
The active ingredient in ZANTAC Injection and ZANTAC
Injection Premixed is ranitidine hydrochloride (HCl), a histamine H2-receptor
antagonist. Chemically it is
N[2-[[[5-[(dimethylamino)methyl]-2-furanyl]methyl]thio]ethyl]-N'-methyl-2-nitro-1,1-ethenediamine,
hydrochloride. It has the following structure:








The empirical formula is C13H22N4O3S•HCl,
representing a molecular weight of 350.87.
Ranitidine HCl is a white to pale yellow, granular substance
that is soluble in water.
ZANTAC Injection is a clear, colorless to yellow,
nonpyrogenic liquid. The yellow color of the liquid tends to intensify without
adversely affecting potency. The pH of the injection solution is 6.7 to 7.3.
Sterile Injection for Intramuscular or Intravenous
Administration
Each 1 mL of aqueous solution contains ranitidine 25 mg (as
the hydrochloride); phenol 5 mg as preservative; and 0.96 mg of monobasic
potassium phosphate and 2.4 mg of dibasic sodium phosphate as buffers.
Sterile, Premixed Solution for Intravenous Administration in
Single-Dose, Flexible Plastic Containers
Each 50 mL contains ranitidine HCl equivalent to 50 mg of
ranitidine, sodium chloride 225 mg, and citric acid 15 mg and dibasic sodium
phosphate 90 mg as buffers in water for injection. It contains no
preservatives. The osmolarity of this solution is 180 mOsm/L (approx.), and the
pH is 6.7 to 7.3.
The flexible plastic container is fabricated from a
specially formulated, nonplasticized, thermoplastic co-polyester (CR3). Water
can permeate from inside the container into the overwrap but not in amounts
sufficient to affect the solution significantly. Solutions inside the plastic
container also can leach out certain of the chemical components in very small
amounts before the expiration period is attained. However, the safety of the
plastic has been confirmed by tests in animals according to USP biological
standards for plastic containers.Last reviewed on RxList: 3/30/2009




Zantac Injection Drug Description
ZANTAC®
(ranitidine hydrochloride) Injection
ZANTAC®
(ranitidine hydrochloride) Injection Premixed
DRUG DESCRIPTION
The active ingredient in ZANTAC Injection and ZANTAC
Injection Premixed is ranitidine hydrochloride (HCl), a histamine H2-receptor
antagonist. Chemically it is
N[2-[[[5-[(dimethylamino)methyl]-2-furanyl]methyl]thio]ethyl]-N'-methyl-2-nitro-1,1-ethenediamine,
hydrochloride. It has the following structure:








The empirical formula is C13H22N4O3S•HCl,
representing a molecular weight of 350.87.
Ranitidine HCl is a white to pale yellow, granular substance
that is soluble in water.
ZANTAC Injection is a clear, colorless to yellow,
nonpyrogenic liquid. The yellow color of the liquid tends to intensify without
adversely affecting potency. The pH of the injection solution is 6.7 to 7.3.
Sterile Injection for Intramuscular or Intravenous
Administration
Each 1 mL of aqueous solution contains ranitidine 25 mg (as
the hydrochloride); phenol 5 mg as preservative; and 0.96 mg of monobasic
potassium phosphate and 2.4 mg of dibasic sodium phosphate as buffers.
Sterile, Premixed Solution for Intravenous Administration in
Single-Dose, Flexible Plastic Containers
Each 50 mL contains ranitidine HCl equivalent to 50 mg of
ranitidine, sodium chloride 225 mg, and citric acid 15 mg and dibasic sodium
phosphate 90 mg as buffers in water for injection. It contains no
preservatives. The osmolarity of this solution is 180 mOsm/L (approx.), and the
pH is 6.7 to 7.3.
The flexible plastic container is fabricated from a
specially formulated, nonplasticized, thermoplastic co-polyester (CR3). Water
can permeate from inside the container into the overwrap but not in amounts
sufficient to affect the solution significantly. Solutions inside the plastic
container also can leach out certain of the chemical components in very small
amounts before the expiration period is attained. However, the safety of the
plastic has been confirmed by tests in animals according to USP biological
standards for plastic containers.Last reviewed on RxList: 3/30/2009




Zantac Injection Drug Description
ZANTAC®
(ranitidine hydrochloride) Injection
ZANTAC®
(ranitidine hydrochloride) Injection Premixed
DRUG DESCRIPTION
The active ingredient in ZANTAC Injection and ZANTAC
Injection Premixed is ranitidine hydrochloride (HCl), a histamine H2-receptor
antagonist. Chemically it is
N[2-[[[5-[(dimethylamino)methyl]-2-furanyl]methyl]thio]ethyl]-N'-methyl-2-nitro-1,1-ethenediamine,
hydrochloride. It has the following structure:








The empirical formula is C13H22N4O3S•HCl,
representing a molecular weight of 350.87.
Ranitidine HCl is a white to pale yellow, granular substance
that is soluble in water.
ZANTAC Injection is a clear, colorless to yellow,
nonpyrogenic liquid. The yellow color of the liquid tends to intensify without
adversely affecting potency. The pH of the injection solution is 6.7 to 7.3.
Sterile Injection for Intramuscular or Intravenous
Administration
Each 1 mL of aqueous solution contains ranitidine 25 mg (as
the hydrochloride); phenol 5 mg as preservative; and 0.96 mg of monobasic
potassium phosphate and 2.4 mg of dibasic sodium phosphate as buffers.
Sterile, Premixed Solution for Intravenous Administration in
Single-Dose, Flexible Plastic Containers
Each 50 mL contains ranitidine HCl equivalent to 50 mg of
ranitidine, sodium chloride 225 mg, and citric acid 15 mg and dibasic sodium
phosphate 90 mg as buffers in water for injection. It contains no
preservatives. The osmolarity of this solution is 180 mOsm/L (approx.), and the
pH is 6.7 to 7.3.
The flexible plastic container is fabricated from a
specially formulated, nonplasticized, thermoplastic co-polyester (CR3). Water
can permeate from inside the container into the overwrap but not in amounts
sufficient to affect the solution significantly. Solutions inside the plastic
container also can leach out certain of the chemical components in very small
amounts before the expiration period is attained. However, the safety of the
plastic has been confirmed by tests in animals according to USP biological
standards for plastic containers.Last reviewed on RxList: 3/30/2009




Zantac Injection Drug Description
ZANTAC®
(ranitidine hydrochloride) Injection
ZANTAC®
(ranitidine hydrochloride) Injection Premixed
DRUG DESCRIPTION
The active ingredient in ZANTAC Injection and ZANTAC
Injection Premixed is ranitidine hydrochloride (HCl), a histamine H2-receptor
antagonist. Chemically it is
N[2-[[[5-[(dimethylamino)methyl]-2-furanyl]methyl]thio]ethyl]-N'-methyl-2-nitro-1,1-ethenediamine,
hydrochloride. It has the following structure:








The empirical formula is C13H22N4O3S•HCl,
representing a molecular weight of 350.87.
Ranitidine HCl is a white to pale yellow, granular substance
that is soluble in water.
ZANTAC Injection is a clear, colorless to yellow,
nonpyrogenic liquid. The yellow color of the liquid tends to intensify without
adversely affecting potency. The pH of the injection solution is 6.7 to 7.3.
Sterile Injection for Intramuscular or Intravenous
Administration
Each 1 mL of aqueous solution contains ranitidine 25 mg (as
the hydrochloride); phenol 5 mg as preservative; and 0.96 mg of monobasic
potassium phosphate and 2.4 mg of dibasic sodium phosphate as buffers.
Sterile, Premixed Solution for Intravenous Administration in
Single-Dose, Flexible Plastic Containers
Each 50 mL contains ranitidine HCl equivalent to 50 mg of
ranitidine, sodium chloride 225 mg, and citric acid 15 mg and dibasic sodium
phosphate 90 mg as buffers in water for injection. It contains no
preservatives. The osmolarity of this solution is 180 mOsm/L (approx.), and the
pH is 6.7 to 7.3.
The flexible plastic container is fabricated from a
specially formulated, nonplasticized, thermoplastic co-polyester (CR3). Water
can permeate from inside the container into the overwrap but not in amounts
sufficient to affect the solution significantly. Solutions inside the plastic
container also can leach out certain of the chemical components in very small
amounts before the expiration period is attained. However, the safety of the
plastic has been confirmed by tests in animals according to USP biological
standards for plastic containers.Last reviewed on RxList: 3/30/2009




Zantac Injection Drug Description
ZANTAC®
(ranitidine hydrochloride) Injection
ZANTAC®
(ranitidine hydrochloride) Injection Premixed
DRUG DESCRIPTION
The active ingredient in ZANTAC Injection and ZANTAC
Injection Premixed is ranitidine hydrochloride (HCl), a histamine H2-receptor
antagonist. Chemically it is
N[2-[[[5-[(dimethylamino)methyl]-2-furanyl]methyl]thio]ethyl]-N'-methyl-2-nitro-1,1-ethenediamine,
hydrochloride. It has the following structure:








The empirical formula is C13H22N4O3S•HCl,
representing a molecular weight of 350.87.
Ranitidine HCl is a white to pale yellow, granular substance
that is soluble in water.
ZANTAC Injection is a clear, colorless to yellow,
nonpyrogenic liquid. The yellow color of the liquid tends to intensify without
adversely affecting potency. The pH of the injection solution is 6.7 to 7.3.
Sterile Injection for Intramuscular or Intravenous
Administration
Each 1 mL of aqueous solution contains ranitidine 25 mg (as
the hydrochloride); phenol 5 mg as preservative; and 0.96 mg of monobasic
potassium phosphate and 2.4 mg of dibasic sodium phosphate as buffers.
Sterile, Premixed Solution for Intravenous Administration in
Single-Dose, Flexible Plastic Containers
Each 50 mL contains ranitidine HCl equivalent to 50 mg of
ranitidine, sodium chloride 225 mg, and citric acid 15 mg and dibasic sodium
phosphate 90 mg as buffers in water for injection. It contains no
preservatives. The osmolarity of this solution is 180 mOsm/L (approx.), and the
pH is 6.7 to 7.3.
The flexible plastic container is fabricated from a
specially formulated, nonplasticized, thermoplastic co-polyester (CR3). Water
can permeate from inside the container into the overwrap but not in amounts
sufficient to affect the solution significantly. Solutions inside the plastic
container also can leach out certain of the chemical components in very small
amounts before the expiration period is attained. However, the safety of the
plastic has been confirmed by tests in animals according to USP biological
standards for plastic containers.Last reviewed on RxList: 3/30/2009





Other reviews about Zantac Injection on wordpress

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  by Day
Last night was a dream.  Simon slept, we slept.  He woke up at 3 hour intervals instead of every half hour.  He ate happily and pooped and slumbered […]


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[caption id="" align="alignnone" width="215" caption="ZANTAC®"][/caption] Ranitidine (INN) is a histamine H2-receptor antagonist that inhibits stomach acid production. It is commonly used in the treatment of peptic ulcer disease (PUD) […]


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It's 5 in the morning and I just walked out of a 24 hour clinic (which I will never go back to again). Siva is a young indian man […]


Det ena avlöser det andra ;)/One thing goes away another one takes over ;)
  by jeanette
English follow Jag och mina demoner *haha* Nu när magkatarren börjar lugna ner sig med hjälp av Zantac så tar muskelsmärtan från Trapezius muskeln över. Trapezius muskeln är belägen i […]


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On Wednesday, Anna had her second chemotherapy treatment. If you are like me, you will have heard of chemotherapy, have some vague idea that it is disagreeable, but […]


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This bed patches to a syndrome of several antacids biased as sorry tumors. Pediatricians of huge reactions feel the lying: For third rigors, risperdal used case medications may […]


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Last night I managed to eat almost a quarter of a sloppy-joe, but the pain was so intense I eventually gave up. Pain killers and Zantac were not […]



Other reviews about Zantac Injection on web:

PRESCRIBING INFORMATION ZANTAC ® (ranitidine hydrochloride) Injection ZANTAC ® (ranitidine hydrochloride) Injection Premixed DESCRIPTION The active ingredient in ZANTAC ... Zantac Injection,Injection Premixed prescribing information


Accurate, FDA approved Zantac Injection information for healthcare professionals and patients - brought to you by Drugs.com. Zantac Injection Official FDA information, side effects and uses.


Consumer information about the medication RANITIDINE INJECTION (Zantac), includes side effects, drug interactions, recommended dosages, and storage information. Read more about ... RANITIDINE INJECTION (Zantac) side effects, medical uses, and drug ...


ZANTAC(R) INJECTION 1 ZANTAC(R) Injection Ranitidine (as hydrochloride) Consumer Medicine Information About your Zantac Injection Read all of this leaflet carefully before you are given ... ZANTAC(R) Injection


Learn about the prescription medication Zantac Injection (Ranitidine Hydrochloride Injection), drug uses, dosage, side effects, drug interactions, warnings, reviews and patient ... Zantac Injection (Ranitidine Hydrochloride Injection) Drug ...


Zantac Injection. Dictionary terms for Zantac Injection in English, English definition for Zantac Injection, Thesaurus and Translations of Zantac Injection to English. Zantac Injection in English - dictionary and translation


ZANTAC INJECTION (Ranitidine) drug information for Duodenal ulcers {DU}, Erosive esophagitis, GERD {GERD}, Hypersecretory conditions~Zollinger-Ellison syndrome, Ulcers, duodenal ... ZANTAC INJECTION (Ranitidine) drug information from MPR


PRESCRIBING INFORMATION ZANTAC ® (ranitidine hydrochloride) Injection Pharmacy Bulk Package—Not for Direct Infusion DESCRIPTION The active ingredient in ZANTAC Injection is ranitidine ... zantac injection 40 mL


SUMMARY The active ingredient in ZANTAC Injection and ZANTAC Injection Premixed is ranitidine hydrochloride (HCl), a histamine H 2-receptor antagonist. Zantac Injection (Ranitidine Injection) - Drug Info, Side Effects ...


ZANTAC INJECTION (Ranitidine) drug information for Duodenal ulcers {DU}, Erosive esophagitis, GERD {GERD}, Hypersecretory conditions~Zollinger-Ellison syndrome, Ulcers, duodenal ... ZANTAC INJECTION (Ranitidine) drug information from MPR - Print ...





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