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Benztropine Mesylate - 66336-776-20 - (benztropine mesylate)

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Drug Information of Benztropine Mesylate

Product NDC: 66336-776
Proprietary Name: Benztropine Mesylate
Non Proprietary Name: benztropine mesylate
Active Ingredient(s): 1    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: 66336-776
Labeler Name: Dispensing Solutions, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040742
Marketing Category: ANDA
Start Marketing Date: 20070827

Package Information of Benztropine Mesylate

Package NDC: 66336-776-20
Package Description: 20 TABLET in 1 BOTTLE, PLASTIC (66336-776-20)

NDC Information of Benztropine Mesylate

NDC Code 66336-776-20
Proprietary Name Benztropine Mesylate
Package Description 20 TABLET in 1 BOTTLE, PLASTIC (66336-776-20)
Product NDC 66336-776
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name benztropine mesylate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070827
Marketing Category Name ANDA
Labeler Name Dispensing Solutions, Inc.
Substance Name BENZTROPINE MESYLATE
Strength Number 1
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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