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Loperamide Hydrochloride - 51079-690-20 - (loperamide hydrochloride)

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Drug Information of Loperamide Hydrochloride

Product NDC: 51079-690
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: 51079-690
Labeler Name: UDL Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072741
Marketing Category: ANDA
Start Marketing Date: 20110727

Package Information of Loperamide Hydrochloride

Package NDC: 51079-690-20
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-690-20) > 1 CAPSULE in 1 BLISTER PACK (51079-690-01)

NDC Information of Loperamide Hydrochloride

NDC Code 51079-690-20
Proprietary Name Loperamide Hydrochloride
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-690-20) > 1 CAPSULE in 1 BLISTER PACK (51079-690-01)
Product NDC 51079-690
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name loperamide hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20110727
Marketing Category Name ANDA
Labeler Name UDL Laboratories, 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


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