Nizatidine - 68788-9838-6 - (Nizatidine)

Alphabetical Index


Drug Information of Nizatidine

Product NDC: 68788-9838
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: 68788-9838
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090618
Marketing Category: ANDA
Start Marketing Date: 20120329

Package Information of Nizatidine

Package NDC: 68788-9838-6
Package Description: 60 CAPSULE in 1 BOTTLE (68788-9838-6)

NDC Information of Nizatidine

NDC Code 68788-9838-6
Proprietary Name Nizatidine
Package Description 60 CAPSULE in 1 BOTTLE (68788-9838-6)
Product NDC 68788-9838
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nizatidine
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20120329
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, 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