Nizatidine - 0591-3137-60 - (Nizatidine)

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Drug Information of Nizatidine

Product NDC: 0591-3137
Proprietary Name: Nizatidine
Non Proprietary Name: Nizatidine
Active Ingredient(s): 150    mg/1 & nbsp;   Nizatidine
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Nizatidine

Product NDC: 0591-3137
Labeler Name: Watson Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075616
Marketing Category: ANDA
Start Marketing Date: 20020709

Package Information of Nizatidine

Package NDC: 0591-3137-60
Package Description: 60 CAPSULE in 1 BOTTLE, PLASTIC (0591-3137-60)

NDC Information of Nizatidine

NDC Code 0591-3137-60
Proprietary Name Nizatidine
Package Description 60 CAPSULE in 1 BOTTLE, PLASTIC (0591-3137-60)
Product NDC 0591-3137
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nizatidine
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20020709
Marketing Category Name ANDA
Labeler Name Watson Laboratories, Inc.
Substance Name NIZATIDINE
Strength Number 150
Strength Unit mg/1
Pharmaceutical Classes Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

Complete Information of Nizatidine


General Information