DEMEROL - 54868-5808-0 - (MEPERIDINE HYDROCHLORIDE)

Alphabetical Index


Drug Information of DEMEROL

Product NDC: 54868-5808
Proprietary Name: DEMEROL
Non Proprietary Name: MEPERIDINE HYDROCHLORIDE
Active Ingredient(s): 50    mg/mL & nbsp;   MEPERIDINE HYDROCHLORIDE
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of DEMEROL

Product NDC: 54868-5808
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021171
Marketing Category: NDA
Start Marketing Date: 20070821

Package Information of DEMEROL

Package NDC: 54868-5808-0
Package Description: 10 CARTRIDGE in 1 BOX (54868-5808-0) > 1 mL in 1 CARTRIDGE

NDC Information of DEMEROL

NDC Code 54868-5808-0
Proprietary Name DEMEROL
Package Description 10 CARTRIDGE in 1 BOX (54868-5808-0) > 1 mL in 1 CARTRIDGE
Product NDC 54868-5808
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name MEPERIDINE HYDROCHLORIDE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Start Marketing Date 20070821
Marketing Category Name NDA
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 DEMEROL


General Information