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Benztropine Mesylate - 0832-1082-00 - (benztropine mesylate)

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Drug Information of Benztropine Mesylate

Product NDC: 0832-1082
Proprietary Name: Benztropine Mesylate
Non Proprietary Name: benztropine mesylate
Active Ingredient(s): 2    mg/1 & nbsp;   benztropine mesylate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Benztropine Mesylate

Product NDC: 0832-1082
Labeler Name: Upsher-Smith Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040103
Marketing Category: ANDA
Start Marketing Date: 19961212

Package Information of Benztropine Mesylate

Package NDC: 0832-1082-00
Package Description: 100 TABLET in 1 BOTTLE (0832-1082-00)

NDC Information of Benztropine Mesylate

NDC Code 0832-1082-00
Proprietary Name Benztropine Mesylate
Package Description 100 TABLET in 1 BOTTLE (0832-1082-00)
Product NDC 0832-1082
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name benztropine mesylate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19961212
Marketing Category Name ANDA
Labeler Name Upsher-Smith Laboratories, Inc.
Substance Name BENZTROPINE MESYLATE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Anticholinergic [EPC],Antihistamine [EPC],Cholinergic Antagonists [MoA],Histamine Receptor Antagonists [MoA]

Complete Information of Benztropine Mesylate


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