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Skelaxin
Skelaxin - 21695-123-30 - (Metaxalone)
Drug Information of Skelaxin
| Product NDC: | 21695-123 |
| Proprietary Name: | Skelaxin |
| 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 Skelaxin
| Product NDC: | 21695-123 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA013217 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19620813 |
Package Information of Skelaxin
| Package NDC: | 21695-123-30 |
| Package Description: | 30 TABLET in 1 BOTTLE (21695-123-30) |
NDC Information of Skelaxin
| NDC Code | 21695-123-30 |
| Proprietary Name | Skelaxin |
| Package Description | 30 TABLET in 1 BOTTLE (21695-123-30) |
| Product NDC | 21695-123 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Metaxalone |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19620813 |
| Marketing Category Name | NDA |
| 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] |
