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Propantheline Bromide - 0054-4721-25 - (Propantheline Bromide)

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Drug Information of Propantheline Bromide

Product NDC: 0054-4721
Proprietary Name: Propantheline Bromide
Non Proprietary Name: Propantheline Bromide
Active Ingredient(s): 15    mg/1 & nbsp;   Propantheline Bromide
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Propantheline Bromide

Product NDC: 0054-4721
Labeler Name: Roxane Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA080927
Marketing Category: ANDA
Start Marketing Date: 19811214

Package Information of Propantheline Bromide

Package NDC: 0054-4721-25
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0054-4721-25)

NDC Information of Propantheline Bromide

NDC Code 0054-4721-25
Proprietary Name Propantheline Bromide
Package Description 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0054-4721-25)
Product NDC 0054-4721
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Propantheline Bromide
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19811214
Marketing Category Name ANDA
Labeler Name Roxane Laboratories, Inc.
Substance Name PROPANTHELINE BROMIDE
Strength Number 15
Strength Unit mg/1
Pharmaceutical Classes Anticholinergic [EPC],Cholinergic Antagonists [MoA]

Complete Information of Propantheline Bromide


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