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Benztropine Mesylate - 43063-267-90 - (Benztropine Mesylate)

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Drug Information of Benztropine Mesylate

Product NDC: 43063-267
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: 43063-267
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089059
Marketing Category: ANDA
Start Marketing Date: 20100228

Package Information of Benztropine Mesylate

Package NDC: 43063-267-90
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC (43063-267-90)

NDC Information of Benztropine Mesylate

NDC Code 43063-267-90
Proprietary Name Benztropine Mesylate
Package Description 90 TABLET in 1 BOTTLE, PLASTIC (43063-267-90)
Product NDC 43063-267
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Benztropine Mesylate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100228
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, 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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