DEMEROL - 54868-4751-1 - (MEPERIDINE HYDROCHLORIDE)

Alphabetical Index


Drug Information of DEMEROL

Product NDC: 54868-4751
Proprietary Name: DEMEROL
Non Proprietary Name: MEPERIDINE HYDROCHLORIDE
Active Ingredient(s): 100    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: 54868-4751
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021171
Marketing Category: NDA
Start Marketing Date: 20030311

Package Information of DEMEROL

Package NDC: 54868-4751-1
Package Description: 1 AMPULE in 1 BOTTLE, DISPENSING (54868-4751-1) > 1 mL in 1 AMPULE

NDC Information of DEMEROL

NDC Code 54868-4751-1
Proprietary Name DEMEROL
Package Description 1 AMPULE in 1 BOTTLE, DISPENSING (54868-4751-1) > 1 mL in 1 AMPULE
Product NDC 54868-4751
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name MEPERIDINE HYDROCHLORIDE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Start Marketing Date 20030311
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name MEPERIDINE HYDROCHLORIDE
Strength Number 100
Strength Unit mg/mL
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of DEMEROL


General Information