Home > National Drug Code (NDC) > MEDIQUE Diamode

MEDIQUE Diamode - 47682-200-33 - (Loperamide Hydrochloride)

Alphabetical Index


Drug Information of MEDIQUE Diamode

Product NDC: 47682-200
Proprietary Name: MEDIQUE Diamode
Non Proprietary Name: Loperamide Hydrochloride
Active Ingredient(s): 2    mg/1 & nbsp;   Loperamide Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of MEDIQUE Diamode

Product NDC: 47682-200
Labeler Name: Unifirst First Aid Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA074091
Marketing Category: ANDA
Start Marketing Date: 20081230

Package Information of MEDIQUE Diamode

Package NDC: 47682-200-33
Package Description: 100 PACKET in 1 BOX, UNIT-DOSE (47682-200-33) > 1 TABLET, FILM COATED in 1 PACKET (47682-200-46)

NDC Information of MEDIQUE Diamode

NDC Code 47682-200-33
Proprietary Name MEDIQUE Diamode
Package Description 100 PACKET in 1 BOX, UNIT-DOSE (47682-200-33) > 1 TABLET, FILM COATED in 1 PACKET (47682-200-46)
Product NDC 47682-200
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Loperamide Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20081230
Marketing Category Name ANDA
Labeler Name Unifirst First Aid Corporation
Substance Name LOPERAMIDE HYDROCHLORIDE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of MEDIQUE Diamode


General Information