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Loperamide Hydrochloride - 0615-0362-39 - (loperamide hydrochloride)

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Drug Information of Loperamide Hydrochloride

Product NDC: 0615-0362
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: 0615-0362
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072741
Marketing Category: ANDA
Start Marketing Date: 20121012

Package Information of Loperamide Hydrochloride

Package NDC: 0615-0362-39
Package Description: 30 CAPSULE in 1 BLISTER PACK (0615-0362-39)

NDC Information of Loperamide Hydrochloride

NDC Code 0615-0362-39
Proprietary Name Loperamide Hydrochloride
Package Description 30 CAPSULE in 1 BLISTER PACK (0615-0362-39)
Product NDC 0615-0362
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name loperamide hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20121012
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
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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