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Loperamide Hydrochloride - 55289-315-08 - (Loperamide Hydrochloride)

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Drug Information of Loperamide Hydrochloride

Product NDC: 55289-315
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: 55289-315
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073192
Marketing Category: ANDA
Start Marketing Date: 20110923

Package Information of Loperamide Hydrochloride

Package NDC: 55289-315-08
Package Description: 8 CAPSULE in 1 BOTTLE, PLASTIC (55289-315-08)

NDC Information of Loperamide Hydrochloride

NDC Code 55289-315-08
Proprietary Name Loperamide Hydrochloride
Package Description 8 CAPSULE in 1 BOTTLE, PLASTIC (55289-315-08)
Product NDC 55289-315
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Loperamide Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20110923
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
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