Lomotil - 0025-0061-51 - (diphenoxylate hydrochloride and atropine sulfate)

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Drug Information of Lomotil

Product NDC: 0025-0061
Proprietary Name: Lomotil
Non Proprietary Name: diphenoxylate hydrochloride and atropine sulfate
Active Ingredient(s): .025; 2.5    mg/1; mg/1 & nbsp;   diphenoxylate hydrochloride and atropine sulfate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Lomotil

Product NDC: 0025-0061
Labeler Name: G.D. Searle LLC Division of Pfizer Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA012462
Marketing Category: NDA
Start Marketing Date: 19600915

Package Information of Lomotil

Package NDC: 0025-0061-51
Package Description: 500 TABLET in 1 BOTTLE (0025-0061-51)

NDC Information of Lomotil

NDC Code 0025-0061-51
Proprietary Name Lomotil
Package Description 500 TABLET in 1 BOTTLE (0025-0061-51)
Product NDC 0025-0061
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name diphenoxylate hydrochloride and atropine sulfate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19600915
Marketing Category Name NDA
Labeler Name G.D. Searle LLC Division of Pfizer 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


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