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Diphenoxylate Hydrochloride and Atropine Sulfate - 55154-6293-9 - (diphenoxylate hydrochloride and atropine sulfate)

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Drug Information of Diphenoxylate Hydrochloride and Atropine Sulfate

Product NDC: 55154-6293
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: 55154-6293
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA085762
Marketing Category: ANDA
Start Marketing Date: 20101130

Package Information of Diphenoxylate Hydrochloride and Atropine Sulfate

Package NDC: 55154-6293-9
Package Description: 30 TABLET in 1 BLISTER PACK (55154-6293-9)

NDC Information of Diphenoxylate Hydrochloride and Atropine Sulfate

NDC Code 55154-6293-9
Proprietary Name Diphenoxylate Hydrochloride and Atropine Sulfate
Package Description 30 TABLET in 1 BLISTER PACK (55154-6293-9)
Product NDC 55154-6293
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name diphenoxylate hydrochloride and atropine sulfate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101130
Marketing Category Name ANDA
Labeler Name Cardinal Health
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


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