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Meperidine Hydrochloride - 42806-051-01 - (Meperidine Hydrochloride)

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Drug Information of Meperidine Hydrochloride

Product NDC: 42806-051
Proprietary Name: Meperidine Hydrochloride
Non Proprietary Name: Meperidine Hydrochloride
Active Ingredient(s): 100    mg/1 & nbsp;   Meperidine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Meperidine Hydrochloride

Product NDC: 42806-051
Labeler Name: Epic Pharma, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040331
Marketing Category: ANDA
Start Marketing Date: 20110505

Package Information of Meperidine Hydrochloride

Package NDC: 42806-051-01
Package Description: 100 TABLET in 1 BOTTLE (42806-051-01)

NDC Information of Meperidine Hydrochloride

NDC Code 42806-051-01
Proprietary Name Meperidine Hydrochloride
Package Description 100 TABLET in 1 BOTTLE (42806-051-01)
Product NDC 42806-051
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Meperidine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110505
Marketing Category Name ANDA
Labeler Name Epic Pharma, LLC
Substance Name MEPERIDINE HYDROCHLORIDE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Meperidine Hydrochloride


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