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Methscopolamine Bromide - 51991-192-60 - (methscopolamine bromide)

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Drug Information of Methscopolamine Bromide

Product NDC: 51991-192
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: 51991-192
Labeler Name: Breckenridge Pharmaceutical, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040642
Marketing Category: ANDA
Start Marketing Date: 20120521

Package Information of Methscopolamine Bromide

Package NDC: 51991-192-60
Package Description: 5 BLISTER PACK in 1 BOX (51991-192-60) > 12 TABLET in 1 BLISTER PACK

NDC Information of Methscopolamine Bromide

NDC Code 51991-192-60
Proprietary Name Methscopolamine Bromide
Package Description 5 BLISTER PACK in 1 BOX (51991-192-60) > 12 TABLET in 1 BLISTER PACK
Product NDC 51991-192
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name methscopolamine bromide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120521
Marketing Category Name ANDA
Labeler Name Breckenridge Pharmaceutical, 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