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Benztropine Mesylate - 0615-7677-31 - (benztropine mesylate)

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Drug Information of Benztropine Mesylate

Product NDC: 0615-7677
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: 0615-7677
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040103
Marketing Category: ANDA
Start Marketing Date: 19961212

Package Information of Benztropine Mesylate

Package NDC: 0615-7677-31
Package Description: 31 TABLET in 1 BLISTER PACK (0615-7677-31)

NDC Information of Benztropine Mesylate

NDC Code 0615-7677-31
Proprietary Name Benztropine Mesylate
Package Description 31 TABLET in 1 BLISTER PACK (0615-7677-31)
Product NDC 0615-7677
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 NCS HealthCare of KY, Inc dba Vangard Labs
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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