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Meperidine Hydrochloride - 54868-3559-1 - (Meperidine Hydrochloride)

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Drug Information of Meperidine Hydrochloride

Product NDC: 54868-3559
Proprietary Name: Meperidine Hydrochloride
Non Proprietary Name: Meperidine Hydrochloride
Active Ingredient(s): 50    mg/mL & nbsp;   Meperidine Hydrochloride
Administration Route(s): INTRAMUSCULAR
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Meperidine Hydrochloride

Product NDC: 54868-3559
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA080455
Marketing Category: ANDA
Start Marketing Date: 20100304

Package Information of Meperidine Hydrochloride

Package NDC: 54868-3559-1
Package Description: 25 VIAL in 1 PACKAGE (54868-3559-1) > 1 mL in 1 VIAL

NDC Information of Meperidine Hydrochloride

NDC Code 54868-3559-1
Proprietary Name Meperidine Hydrochloride
Package Description 25 VIAL in 1 PACKAGE (54868-3559-1) > 1 mL in 1 VIAL
Product NDC 54868-3559
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Meperidine Hydrochloride
Dosage Form Name INJECTION
Route Name INTRAMUSCULAR
Start Marketing Date 20100304
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name MEPERIDINE HYDROCHLORIDE
Strength Number 50
Strength Unit mg/mL
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Meperidine Hydrochloride


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