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Methscopolamine Bromide - 64376-604-61 - (Methscopolamine Bromide)

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Drug Information of Methscopolamine Bromide

Product NDC: 64376-604
Proprietary Name: Methscopolamine Bromide
Non Proprietary Name: Methscopolamine Bromide
Active Ingredient(s): 5    mg/1 & nbsp;   Methscopolamine Bromide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Methscopolamine Bromide

Product NDC: 64376-604
Labeler Name: Boca Pharmacal, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040624
Marketing Category: ANDA
Start Marketing Date: 20061228

Package Information of Methscopolamine Bromide

Package NDC: 64376-604-61
Package Description: 60 TABLET in 1 BOTTLE (64376-604-61)

NDC Information of Methscopolamine Bromide

NDC Code 64376-604-61
Proprietary Name Methscopolamine Bromide
Package Description 60 TABLET in 1 BOTTLE (64376-604-61)
Product NDC 64376-604
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Methscopolamine Bromide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20061228
Marketing Category Name ANDA
Labeler Name Boca Pharmacal, Inc.
Substance Name METHSCOPOLAMINE BROMIDE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Anticholinergic [EPC],Cholinergic Antagonists [MoA]

Complete Information of Methscopolamine Bromide


General Information