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Benztropine Mesylate - 50111-393-03 - (Benztropine Mesylate)

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Drug Information of Benztropine Mesylate

Product NDC: 50111-393
Proprietary Name: Benztropine Mesylate
Non Proprietary Name: Benztropine Mesylate
Active Ingredient(s): .5    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: 50111-393
Labeler Name: Pliva Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089058
Marketing Category: ANDA
Start Marketing Date: 19900930

Package Information of Benztropine Mesylate

Package NDC: 50111-393-03
Package Description: 1000 TABLET in 1 BOTTLE (50111-393-03)

NDC Information of Benztropine Mesylate

NDC Code 50111-393-03
Proprietary Name Benztropine Mesylate
Package Description 1000 TABLET in 1 BOTTLE (50111-393-03)
Product NDC 50111-393
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Benztropine Mesylate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19900930
Marketing Category Name ANDA
Labeler Name Pliva Inc.
Substance Name BENZTROPINE MESYLATE
Strength Number .5
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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