Imodium - 50580-134-44 - (Loperamide Hydrochloride)

Alphabetical Index


Drug Information of Imodium

Product NDC: 50580-134
Proprietary Name: Imodium
Non Proprietary Name: Loperamide Hydrochloride
Active Ingredient(s): 1    mg/7.5mL & nbsp;   Loperamide Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Imodium

Product NDC: 50580-134
Labeler Name: McNeil Consumer Healthcare Div McNeil-PPC, Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA019487
Marketing Category: NDA
Start Marketing Date: 20050101

Package Information of Imodium

Package NDC: 50580-134-44
Package Description: 120 mL in 1 BOTTLE (50580-134-44)

NDC Information of Imodium

NDC Code 50580-134-44
Proprietary Name Imodium
Package Description 120 mL in 1 BOTTLE (50580-134-44)
Product NDC 50580-134
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Loperamide Hydrochloride
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20050101
Marketing Category Name NDA
Labeler Name McNeil Consumer Healthcare Div McNeil-PPC, Inc
Substance Name LOPERAMIDE HYDROCHLORIDE
Strength Number 1
Strength Unit mg/7.5mL
Pharmaceutical Classes

Complete Information of Imodium


General Information