Motofen - 0187-0500-02 - (difenoxin hydrochloride)

Alphabetical Index


Drug Information of Motofen

Product NDC: 0187-0500
Proprietary Name: Motofen
Non Proprietary Name: difenoxin hydrochloride
Active Ingredient(s): .025; 1    mg/1; mg/1 & nbsp;   difenoxin hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Motofen

Product NDC: 0187-0500
Labeler Name: Valeant Pharmaceuticals North America LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA017744
Marketing Category: NDA
Start Marketing Date: 19620714

Package Information of Motofen

Package NDC: 0187-0500-02
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC (0187-0500-02)

NDC Information of Motofen

NDC Code 0187-0500-02
Proprietary Name Motofen
Package Description 100 TABLET in 1 BOTTLE, PLASTIC (0187-0500-02)
Product NDC 0187-0500
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name difenoxin hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19620714
Marketing Category Name NDA
Labeler Name Valeant Pharmaceuticals North America LLC
Substance Name ATROPINE SULFATE; DIFENOXIN HYDROCHLORIDE
Strength Number .025; 1
Strength Unit mg/1; mg/1
Pharmaceutical Classes Antidiarrheal [EPC],Anticholinergic [EPC],Cholinergic Antagonists [MoA],Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA]

Complete Information of Motofen


General Information