Home > National Drug Code (NDC) > Orphenadrine Citrate

Orphenadrine Citrate - 17478-538-02 - (Orphenadrine Citrate)

Alphabetical Index


Drug Information of Orphenadrine Citrate

Product NDC: 17478-538
Proprietary Name: Orphenadrine Citrate
Non Proprietary Name: Orphenadrine Citrate
Active Ingredient(s): 30    mg/mL & nbsp;   Orphenadrine Citrate
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Orphenadrine Citrate

Product NDC: 17478-538
Labeler Name: Akorn, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040484
Marketing Category: ANDA
Start Marketing Date: 20061017

Package Information of Orphenadrine Citrate

Package NDC: 17478-538-02
Package Description: 10 VIAL in 1 CARTON (17478-538-02) > 2 mL in 1 VIAL

NDC Information of Orphenadrine Citrate

NDC Code 17478-538-02
Proprietary Name Orphenadrine Citrate
Package Description 10 VIAL in 1 CARTON (17478-538-02) > 2 mL in 1 VIAL
Product NDC 17478-538
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Orphenadrine Citrate
Dosage Form Name INJECTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20061017
Marketing Category Name ANDA
Labeler Name Akorn, Inc.
Substance Name ORPHENADRINE CITRATE
Strength Number 30
Strength Unit mg/mL
Pharmaceutical Classes Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]

Complete Information of Orphenadrine Citrate


General Information