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Metaxalone
Metaxalone - 21695-585-90 - (Metaxalone)
Drug Information of Metaxalone
| Product NDC: | 21695-585 |
| Proprietary Name: | Metaxalone |
| Non Proprietary Name: | Metaxalone |
| Active Ingredient(s): | 800 mg/1 & nbsp; Metaxalone |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Metaxalone
| Product NDC: | 21695-585 |
| Labeler Name: | Rebel Distributors Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040445 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100331 |
Package Information of Metaxalone
| Package NDC: | 21695-585-90 |
| Package Description: | 90 TABLET in 1 BOTTLE (21695-585-90) |
NDC Information of Metaxalone
| NDC Code | 21695-585-90 |
| Proprietary Name | Metaxalone |
| Package Description | 90 TABLET in 1 BOTTLE (21695-585-90) |
| Product NDC | 21695-585 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Metaxalone |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100331 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp. |
| Substance Name | METAXALONE |
| Strength Number | 800 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC] |
