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Benztropine Mesylate - 55154-5096-0 - (benztropine mesylate)

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Drug Information of Benztropine Mesylate

Product NDC: 55154-5096
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: 55154-5096
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040742
Marketing Category: ANDA
Start Marketing Date: 20091016

Package Information of Benztropine Mesylate

Package NDC: 55154-5096-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-5096-0) > 1 TABLET in 1 BLISTER PACK

NDC Information of Benztropine Mesylate

NDC Code 55154-5096-0
Proprietary Name Benztropine Mesylate
Package Description 10 BLISTER PACK in 1 BAG (55154-5096-0) > 1 TABLET in 1 BLISTER PACK
Product NDC 55154-5096
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name benztropine mesylate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091016
Marketing Category Name ANDA
Labeler Name Cardinal Health
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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