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Ranitidine Hydrochloride - 65841-763-02 - (Ranitidine Hydrochloride)

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Drug Information of Ranitidine Hydrochloride

Product NDC: 65841-763
Proprietary Name: Ranitidine Hydrochloride
Non Proprietary Name: Ranitidine Hydrochloride
Active Ingredient(s): 25    mg/mL & nbsp;   Ranitidine Hydrochloride
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ranitidine Hydrochloride

Product NDC: 65841-763
Labeler Name: Cadila Healthcare Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091534
Marketing Category: ANDA
Start Marketing Date: 20130301

Package Information of Ranitidine Hydrochloride

Package NDC: 65841-763-02
Package Description: 10 VIAL in 1 CARTON (65841-763-02) > 2 mL in 1 VIAL

NDC Information of Ranitidine Hydrochloride

NDC Code 65841-763-02
Proprietary Name Ranitidine Hydrochloride
Package Description 10 VIAL in 1 CARTON (65841-763-02) > 2 mL in 1 VIAL
Product NDC 65841-763
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ranitidine Hydrochloride
Dosage Form Name INJECTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20130301
Marketing Category Name ANDA
Labeler Name Cadila Healthcare Limited
Substance Name RANITIDINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/mL
Pharmaceutical Classes Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

Complete Information of Ranitidine Hydrochloride


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