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Benztropine Mesylate - 14789-300-02 - (BENZTROPINE MESYLATE)

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Drug Information of Benztropine Mesylate

Product NDC: 14789-300
Proprietary Name: Benztropine Mesylate
Non Proprietary Name: BENZTROPINE MESYLATE
Active Ingredient(s): 1    mg/mL & nbsp;   BENZTROPINE MESYLATE
Administration Route(s): PARENTERAL
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Benztropine Mesylate

Product NDC: 14789-300
Labeler Name: Nexus Pharmaceuticals Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090233
Marketing Category: ANDA
Start Marketing Date: 20090729

Package Information of Benztropine Mesylate

Package NDC: 14789-300-02
Package Description: 5 VIAL in 1 PACKAGE (14789-300-02) > 2 mL in 1 VIAL

NDC Information of Benztropine Mesylate

NDC Code 14789-300-02
Proprietary Name Benztropine Mesylate
Package Description 5 VIAL in 1 PACKAGE (14789-300-02) > 2 mL in 1 VIAL
Product NDC 14789-300
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name BENZTROPINE MESYLATE
Dosage Form Name INJECTION
Route Name PARENTERAL
Start Marketing Date 20090729
Marketing Category Name ANDA
Labeler Name Nexus Pharmaceuticals Inc
Substance Name BENZTROPINE MESYLATE
Strength Number 1
Strength Unit mg/mL
Pharmaceutical Classes Anticholinergic [EPC],Antihistamine [EPC],Cholinergic Antagonists [MoA],Histamine Receptor Antagonists [MoA]

Complete Information of Benztropine Mesylate


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