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Benztropine Mesylate - 49349-231-02 - (Benztropine Mesylate)

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Drug Information of Benztropine Mesylate

Product NDC: 49349-231
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: 49349-231
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072266
Marketing Category: ANDA
Start Marketing Date: 20110314

Package Information of Benztropine Mesylate

Package NDC: 49349-231-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-231-02)

NDC Information of Benztropine Mesylate

NDC Code 49349-231-02
Proprietary Name Benztropine Mesylate
Package Description 30 TABLET in 1 BLISTER PACK (49349-231-02)
Product NDC 49349-231
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Benztropine Mesylate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110314
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
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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