Norflex - 29336-540-06 - (orphenadrine citrate)

Alphabetical Index


Drug Information of Norflex

Product NDC: 29336-540
Proprietary Name: Norflex
Non Proprietary Name: orphenadrine citrate
Active Ingredient(s): 60    mg/2mL & nbsp;   orphenadrine citrate
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Norflex

Product NDC: 29336-540
Labeler Name: Graceway Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA013055
Marketing Category: NDA
Start Marketing Date: 20100525

Package Information of Norflex

Package NDC: 29336-540-06
Package Description: 6 AMPULE in 1 BOX (29336-540-06) > 2 mL in 1 AMPULE

NDC Information of Norflex

NDC Code 29336-540-06
Proprietary Name Norflex
Package Description 6 AMPULE in 1 BOX (29336-540-06) > 2 mL in 1 AMPULE
Product NDC 29336-540
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name orphenadrine citrate
Dosage Form Name INJECTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20100525
Marketing Category Name NDA
Labeler Name Graceway Pharmaceuticals, LLC
Substance Name ORPHENADRINE CITRATE
Strength Number 60
Strength Unit mg/2mL
Pharmaceutical Classes Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]

Complete Information of Norflex


General Information