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BACLOFEN
BACLOFEN - 16590-026-72 - (BACLOFEN)
Drug Information of BACLOFEN
| Product NDC: | 16590-026 |
| Proprietary Name: | BACLOFEN |
| Non Proprietary Name: | BACLOFEN |
| Active Ingredient(s): | 10 mg/1 & nbsp; BACLOFEN |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of BACLOFEN
| Product NDC: | 16590-026 |
| Labeler Name: | STAT RX USA LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA072824 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19910918 |
Package Information of BACLOFEN
| Package NDC: | 16590-026-72 |
| Package Description: | 120 TABLET in 1 BOTTLE (16590-026-72) |
NDC Information of BACLOFEN
| NDC Code | 16590-026-72 |
| Proprietary Name | BACLOFEN |
| Package Description | 120 TABLET in 1 BOTTLE (16590-026-72) |
| Product NDC | 16590-026 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | BACLOFEN |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19910918 |
| Marketing Category Name | ANDA |
| Labeler Name | STAT RX USA LLC |
| Substance Name | BACLOFEN |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | GABA A Agonists [MoA],GABA B Agonists [MoA],gamma-Aminobutyric Acid-ergic Agonist [EPC] |
