nizatidine - 0185-0300-01 - (nizatidine)

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Drug Information of nizatidine

Product NDC: 0185-0300
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: 0185-0300
Labeler Name: Eon Labs, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076178
Marketing Category: ANDA
Start Marketing Date: 20020705

Package Information of nizatidine

Package NDC: 0185-0300-01
Package Description: 100 CAPSULE in 1 BOTTLE (0185-0300-01)

NDC Information of nizatidine

NDC Code 0185-0300-01
Proprietary Name nizatidine
Package Description 100 CAPSULE in 1 BOTTLE (0185-0300-01)
Product NDC 0185-0300
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name nizatidine
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20020705
Marketing Category Name ANDA
Labeler Name Eon Labs, Inc.
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