IMODIUM - 50580-295-84 - (Loperamide hydrochloride)

Alphabetical Index


Drug Information of IMODIUM

Product NDC: 50580-295
Proprietary Name: IMODIUM
Non Proprietary Name: Loperamide hydrochloride
Active Ingredient(s): 2    mg/1 & nbsp;   Loperamide hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of IMODIUM

Product NDC: 50580-295
Labeler Name: McNeil Consumer Healthcare Div McNeil-PPC, Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA019860
Marketing Category: NDA
Start Marketing Date: 19891201

Package Information of IMODIUM

Package NDC: 50580-295-84
Package Description: 8 BLISTER PACK in 1 CARTON (50580-295-84) > 6 TABLET in 1 BLISTER PACK

NDC Information of IMODIUM

NDC Code 50580-295-84
Proprietary Name IMODIUM
Package Description 8 BLISTER PACK in 1 CARTON (50580-295-84) > 6 TABLET in 1 BLISTER PACK
Product NDC 50580-295
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Loperamide hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19891201
Marketing Category Name NDA
Labeler Name McNeil Consumer Healthcare Div McNeil-PPC, Inc
Substance Name LOPERAMIDE HYDROCHLORIDE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of IMODIUM


General Information