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

Diphenoxylate Hydrochloride and Atropine Sulfate - 49884-771-10 - (Diphenoxylate Hydrochloride and Atropine Sulfate)

Alphabetical Index


Drug Information of Diphenoxylate Hydrochloride and Atropine Sulfate

Product NDC: 49884-771
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: 49884-771
Labeler Name: Par Pharmaceutical, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040357
Marketing Category: ANDA
Start Marketing Date: 20000526

Package Information of Diphenoxylate Hydrochloride and Atropine Sulfate

Package NDC: 49884-771-10
Package Description: 1000 TABLET in 1 BOTTLE (49884-771-10)

NDC Information of Diphenoxylate Hydrochloride and Atropine Sulfate

NDC Code 49884-771-10
Proprietary Name Diphenoxylate Hydrochloride and Atropine Sulfate
Package Description 1000 TABLET in 1 BOTTLE (49884-771-10)
Product NDC 49884-771
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diphenoxylate Hydrochloride and Atropine Sulfate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20000526
Marketing Category Name ANDA
Labeler Name Par Pharmaceutical, 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 Diphenoxylate Hydrochloride and Atropine Sulfate


General Information