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Meperidine Hydrochloride - 54868-1233-2 - (Meperidine Hydrochloride)

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Drug Information of Meperidine Hydrochloride

Product NDC: 54868-1233
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: 54868-1233
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040191
Marketing Category: ANDA
Start Marketing Date: 20090914

Package Information of Meperidine Hydrochloride

Package NDC: 54868-1233-2
Package Description: 40 TABLET in 1 BOTTLE, PLASTIC (54868-1233-2)

NDC Information of Meperidine Hydrochloride

NDC Code 54868-1233-2
Proprietary Name Meperidine Hydrochloride
Package Description 40 TABLET in 1 BOTTLE, PLASTIC (54868-1233-2)
Product NDC 54868-1233
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Meperidine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090914
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
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