Nizatidine - 68462-426-01 - (Nizatidine)

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Drug Information of Nizatidine

Product NDC: 68462-426
Proprietary Name: Nizatidine
Non Proprietary Name: Nizatidine
Active Ingredient(s): 300    mg/1 & nbsp;   Nizatidine
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Nizatidine

Product NDC: 68462-426
Labeler Name: Glenmark Generics Inc.,USA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090618
Marketing Category: ANDA
Start Marketing Date: 20110715

Package Information of Nizatidine

Package NDC: 68462-426-01
Package Description: 100 CAPSULE in 1 BOTTLE (68462-426-01)

NDC Information of Nizatidine

NDC Code 68462-426-01
Proprietary Name Nizatidine
Package Description 100 CAPSULE in 1 BOTTLE (68462-426-01)
Product NDC 68462-426
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nizatidine
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20110715
Marketing Category Name ANDA
Labeler Name Glenmark Generics Inc.,USA
Substance Name NIZATIDINE
Strength Number 300
Strength Unit mg/1
Pharmaceutical Classes Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

Complete Information of Nizatidine


General Information