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Loperamide Hydrochloride - 55154-4944-5 - (Loperamide Hydrochloride)

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Drug Information of Loperamide Hydrochloride

Product NDC: 55154-4944
Proprietary Name: Loperamide Hydrochloride
Non Proprietary Name: Loperamide Hydrochloride
Active Ingredient(s): 2    mg/10mL & nbsp;   Loperamide Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Loperamide Hydrochloride

Product NDC: 55154-4944
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073079
Marketing Category: ANDA
Start Marketing Date: 19920430

Package Information of Loperamide Hydrochloride

Package NDC: 55154-4944-5
Package Description: 5 CUP, UNIT-DOSE in 1 BAG (55154-4944-5) > 10 mL in 1 CUP, UNIT-DOSE

NDC Information of Loperamide Hydrochloride

NDC Code 55154-4944-5
Proprietary Name Loperamide Hydrochloride
Package Description 5 CUP, UNIT-DOSE in 1 BAG (55154-4944-5) > 10 mL in 1 CUP, UNIT-DOSE
Product NDC 55154-4944
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Loperamide Hydrochloride
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 19920430
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name LOPERAMIDE HYDROCHLORIDE
Strength Number 2
Strength Unit mg/10mL
Pharmaceutical Classes Opioid Agonist [EPC],Opioid Agonists [MoA]

Complete Information of Loperamide Hydrochloride


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