Lomotil - 54868-0427-5 - (Diphenoxylate Hydrochloride)

Alphabetical Index


Drug Information of Lomotil

Product NDC: 54868-0427
Proprietary Name: Lomotil
Non Proprietary Name: Diphenoxylate Hydrochloride
Active Ingredient(s): .025; 2.5    mg/1; mg/1 & nbsp;   Diphenoxylate Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Lomotil

Product NDC: 54868-0427
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA012462
Marketing Category: NDA
Start Marketing Date: 20090119

Package Information of Lomotil

Package NDC: 54868-0427-5
Package Description: 10 TABLET in 1 BOTTLE (54868-0427-5)

NDC Information of Lomotil

NDC Code 54868-0427-5
Proprietary Name Lomotil
Package Description 10 TABLET in 1 BOTTLE (54868-0427-5)
Product NDC 54868-0427
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diphenoxylate Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090119
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE
Strength Number .025; 2.5
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 Lomotil


General Information