Home > National Drug Code (NDC) > Diphenoxylate Hydrochloride and Atropine Sulfate

Diphenoxylate Hydrochloride and Atropine Sulfate - 59762-1061-1 - (DIPHENOXYLATE HYDROCHLORIDE and ATROPINE SULFATE)

Alphabetical Index


Drug Information of Diphenoxylate Hydrochloride and Atropine Sulfate

Product NDC: 59762-1061
Proprietary Name: Diphenoxylate Hydrochloride and Atropine Sulfate
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 Diphenoxylate Hydrochloride and Atropine Sulfate

Product NDC: 59762-1061
Labeler Name: Greenstone LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA012462
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20130227

Package Information of Diphenoxylate Hydrochloride and Atropine Sulfate

Package NDC: 59762-1061-1
Package Description: 100 TABLET in 1 BOTTLE (59762-1061-1)

NDC Information of Diphenoxylate Hydrochloride and Atropine Sulfate

NDC Code 59762-1061-1
Proprietary Name Diphenoxylate Hydrochloride and Atropine Sulfate
Package Description 100 TABLET in 1 BOTTLE (59762-1061-1)
Product NDC 59762-1061
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name DIPHENOXYLATE HYDROCHLORIDE and ATROPINE SULFATE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130227
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Greenstone LLC
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 Diphenoxylate Hydrochloride and Atropine Sulfate


General Information