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Meperidine Hydrochloride - 63629-4549-1 - (Meperidine Hydrochloride)

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Drug Information of Meperidine Hydrochloride

Product NDC: 63629-4549
Proprietary Name: Meperidine Hydrochloride
Non Proprietary Name: Meperidine Hydrochloride
Active Ingredient(s): 50    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: 63629-4549
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040191
Marketing Category: ANDA
Start Marketing Date: 19981217

Package Information of Meperidine Hydrochloride

Package NDC: 63629-4549-1
Package Description: 30 TABLET in 1 BOTTLE (63629-4549-1)

NDC Information of Meperidine Hydrochloride

NDC Code 63629-4549-1
Proprietary Name Meperidine Hydrochloride
Package Description 30 TABLET in 1 BOTTLE (63629-4549-1)
Product NDC 63629-4549
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Meperidine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19981217
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name MEPERIDINE HYDROCHLORIDE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Meperidine Hydrochloride


General Information