Product NDC: | 58281-560 |
Proprietary Name: | Lioresal |
Non Proprietary Name: | baclofen |
Active Ingredient(s): | .5 mg/mL & nbsp; baclofen |
Administration Route(s): | INTRATHECAL |
Dosage Form(s): | INJECTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 58281-560 |
Labeler Name: | Medtronic Neuromodulation |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020075 |
Marketing Category: | NDA |
Start Marketing Date: | 19920617 |
Package NDC: | 58281-560-02 |
Package Description: | 2 AMPULE in 1 PACKAGE, COMBINATION (58281-560-02) > 20 mL in 1 AMPULE |
NDC Code | 58281-560-02 |
Proprietary Name | Lioresal |
Package Description | 2 AMPULE in 1 PACKAGE, COMBINATION (58281-560-02) > 20 mL in 1 AMPULE |
Product NDC | 58281-560 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | baclofen |
Dosage Form Name | INJECTION |
Route Name | INTRATHECAL |
Start Marketing Date | 19920617 |
Marketing Category Name | NDA |
Labeler Name | Medtronic Neuromodulation |
Substance Name | BACLOFEN |
Strength Number | .5 |
Strength Unit | mg/mL |
Pharmaceutical Classes | GABA A Agonists [MoA],GABA B Agonists [MoA],gamma-Aminobutyric Acid-ergic Agonist [EPC] |