Home > National Drug Code (NDC) > Loperamide Hydrochloride

Loperamide Hydrochloride - 21695-692-15 - (Loperamide Hydrochloride)

Alphabetical Index


Drug Information of Loperamide Hydrochloride

Product NDC: 21695-692
Proprietary Name: Loperamide Hydrochloride
Non Proprietary Name: Loperamide Hydrochloride
Active Ingredient(s): 2    mg/1 & nbsp;   Loperamide Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Loperamide Hydrochloride

Product NDC: 21695-692
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073192
Marketing Category: ANDA
Start Marketing Date: 19920430

Package Information of Loperamide Hydrochloride

Package NDC: 21695-692-15
Package Description: 15 CAPSULE in 1 BOTTLE (21695-692-15)

NDC Information of Loperamide Hydrochloride

NDC Code 21695-692-15
Proprietary Name Loperamide Hydrochloride
Package Description 15 CAPSULE in 1 BOTTLE (21695-692-15)
Product NDC 21695-692
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Loperamide Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19920430
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name LOPERAMIDE HYDROCHLORIDE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Opioid Agonist [EPC],Opioid Agonists [MoA]

Complete Information of Loperamide Hydrochloride


General Information