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Benztropine Mesylate - 51079-406-20 - (benztropine mesylate)

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Drug Information of Benztropine Mesylate

Product NDC: 51079-406
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: 51079-406
Labeler Name: UDL Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040742
Marketing Category: ANDA
Start Marketing Date: 20091016

Package Information of Benztropine Mesylate

Package NDC: 51079-406-20
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-406-20) > 1 TABLET in 1 BLISTER PACK (51079-406-01)

NDC Information of Benztropine Mesylate

NDC Code 51079-406-20
Proprietary Name Benztropine Mesylate
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-406-20) > 1 TABLET in 1 BLISTER PACK (51079-406-01)
Product NDC 51079-406
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 UDL Laboratories, 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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