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Ranitidine Hydrochloride - 21695-338-30 - (Ranitidine Hydrochloride)

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Drug Information of Ranitidine Hydrochloride

Product NDC: 21695-338
Proprietary Name: Ranitidine Hydrochloride
Non Proprietary Name: Ranitidine Hydrochloride
Active Ingredient(s): 300    mg/1 & nbsp;   Ranitidine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Ranitidine Hydrochloride

Product NDC: 21695-338
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074655
Marketing Category: ANDA
Start Marketing Date: 19971022

Package Information of Ranitidine Hydrochloride

Package NDC: 21695-338-30
Package Description: 30 CAPSULE in 1 BOTTLE (21695-338-30)

NDC Information of Ranitidine Hydrochloride

NDC Code 21695-338-30
Proprietary Name Ranitidine Hydrochloride
Package Description 30 CAPSULE in 1 BOTTLE (21695-338-30)
Product NDC 21695-338
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ranitidine Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19971022
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name RANITIDINE HYDROCHLORIDE
Strength Number 300
Strength Unit mg/1
Pharmaceutical Classes Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

Complete Information of Ranitidine Hydrochloride


General Information