Ofirmev - 43825-102-01 - (acetaminophen)

Alphabetical Index


Drug Information of Ofirmev

Product NDC: 43825-102
Proprietary Name: Ofirmev
Non Proprietary Name: acetaminophen
Active Ingredient(s): 10    mg/mL & nbsp;   acetaminophen
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ofirmev

Product NDC: 43825-102
Labeler Name: Cadence Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022450
Marketing Category: NDA
Start Marketing Date: 20101108

Package Information of Ofirmev

Package NDC: 43825-102-01
Package Description: 24 VIAL, GLASS in 1 CARTON (43825-102-01) > 100 mL in 1 VIAL, GLASS

NDC Information of Ofirmev

NDC Code 43825-102-01
Proprietary Name Ofirmev
Package Description 24 VIAL, GLASS in 1 CARTON (43825-102-01) > 100 mL in 1 VIAL, GLASS
Product NDC 43825-102
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name acetaminophen
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20101108
Marketing Category Name NDA
Labeler Name Cadence Pharmaceuticals, Inc.
Substance Name ACETAMINOPHEN
Strength Number 10
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of Ofirmev


General Information