Imodium - 50580-397-20 - (Loperamide hydrochloride)

Alphabetical Index


Drug Information of Imodium

Product NDC: 50580-397
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, CHEWABLE
Coding System: National Drug Codes(NDC)

Labeler Information of Imodium

Product NDC: 50580-397
Labeler Name: McNeil Consumer Healthcare Div. McNeil-PPC, Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA020448
Marketing Category: NDA
Start Marketing Date: 20070201

Package Information of Imodium

Package NDC: 50580-397-20
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (50580-397-20) > 20 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC

NDC Information of Imodium

NDC Code 50580-397-20
Proprietary Name Imodium
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (50580-397-20) > 20 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC
Product NDC 50580-397
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Loperamide hydrochloride
Dosage Form Name TABLET, CHEWABLE
Route Name ORAL
Start Marketing Date 20070201
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