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Loperamide Hydrochloride - 55154-6223-9 - (Loperamide Hydrochloride)

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Drug Information of Loperamide Hydrochloride

Product NDC: 55154-6223
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: 55154-6223
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072741
Marketing Category: ANDA
Start Marketing Date: 19910918

Package Information of Loperamide Hydrochloride

Package NDC: 55154-6223-9
Package Description: 6 BLISTER PACK in 1 CARTON (55154-6223-9) > 5 CAPSULE in 1 BLISTER PACK

NDC Information of Loperamide Hydrochloride

NDC Code 55154-6223-9
Proprietary Name Loperamide Hydrochloride
Package Description 6 BLISTER PACK in 1 CARTON (55154-6223-9) > 5 CAPSULE in 1 BLISTER PACK
Product NDC 55154-6223
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Loperamide Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19910918
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name LOPERAMIDE HYDROCHLORIDE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Opioid Agonist [EPC],Opioid Agonists [MoA]

Complete Information of Loperamide Hydrochloride


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