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BENZTROPINE MESYLATE - 21695-286-30 - (BENZTROPINE MESYLATE)

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Drug Information of BENZTROPINE MESYLATE

Product NDC: 21695-286
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: 21695-286
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072266
Marketing Category: ANDA
Start Marketing Date: 20020813

Package Information of BENZTROPINE MESYLATE

Package NDC: 21695-286-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (21695-286-30)

NDC Information of BENZTROPINE MESYLATE

NDC Code 21695-286-30
Proprietary Name BENZTROPINE MESYLATE
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (21695-286-30)
Product NDC 21695-286
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name BENZTROPINE MESYLATE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20020813
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
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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