Nizatidine - 60505-0230-2 - (Nizatidine)

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Drug Information of Nizatidine

Product NDC: 60505-0230
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: 60505-0230
Labeler Name: Apotex Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076383
Marketing Category: ANDA
Start Marketing Date: 20030601

Package Information of Nizatidine

Package NDC: 60505-0230-2
Package Description: 1000 CAPSULE in 1 BOTTLE (60505-0230-2)

NDC Information of Nizatidine

NDC Code 60505-0230-2
Proprietary Name Nizatidine
Package Description 1000 CAPSULE in 1 BOTTLE (60505-0230-2)
Product NDC 60505-0230
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nizatidine
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20030601
Marketing Category Name ANDA
Labeler Name Apotex Corp
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