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Benztropine Mesylate - 68084-381-01 - (Benztropine Mesylate)

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Drug Information of Benztropine Mesylate

Product NDC: 68084-381
Proprietary Name: Benztropine Mesylate
Non Proprietary Name: Benztropine Mesylate
Active Ingredient(s): .5    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: 68084-381
Labeler Name: American Health Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040738
Marketing Category: ANDA
Start Marketing Date: 20100114

Package Information of Benztropine Mesylate

Package NDC: 68084-381-01
Package Description: 10 BLISTER PACK in 1 CARTON (68084-381-01) > 10 TABLET in 1 BLISTER PACK (68084-381-11)

NDC Information of Benztropine Mesylate

NDC Code 68084-381-01
Proprietary Name Benztropine Mesylate
Package Description 10 BLISTER PACK in 1 CARTON (68084-381-01) > 10 TABLET in 1 BLISTER PACK (68084-381-11)
Product NDC 68084-381
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Benztropine Mesylate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100114
Marketing Category Name ANDA
Labeler Name American Health Packaging
Substance Name BENZTROPINE MESYLATE
Strength Number .5
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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