IMODIUM - 50580-338-24 - (loperamide hydrochloride and dimethicone)

Alphabetical Index


Drug Information of IMODIUM

Product NDC: 50580-338
Proprietary Name: IMODIUM
Non Proprietary Name: loperamide hydrochloride and dimethicone
Active Ingredient(s): 125; 2    mg/1; mg/1 & nbsp;   loperamide hydrochloride and dimethicone
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of IMODIUM

Product NDC: 50580-338
Labeler Name: McNeil Consumer Healthcare Div. McNeil-PPC, Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA021140
Marketing Category: NDA
Start Marketing Date: 20080701

Package Information of IMODIUM

Package NDC: 50580-338-24
Package Description: 4 BLISTER PACK in 1 CARTON (50580-338-24) > 6 TABLET in 1 BLISTER PACK

NDC Information of IMODIUM

NDC Code 50580-338-24
Proprietary Name IMODIUM
Package Description 4 BLISTER PACK in 1 CARTON (50580-338-24) > 6 TABLET in 1 BLISTER PACK
Product NDC 50580-338
Product Type Name HUMAN OTC DRUG
Non Proprietary Name loperamide hydrochloride and dimethicone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080701
Marketing Category Name NDA
Labeler Name McNeil Consumer Healthcare Div. McNeil-PPC, Inc
Substance Name DIMETHICONE; LOPERAMIDE HYDROCHLORIDE
Strength Number 125; 2
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of IMODIUM


General Information