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METAXALONE
METAXALONE - 16590-346-40 - (METAXALONE)
Drug Information of METAXALONE
| Product NDC: | 16590-346 |
| 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: | 16590-346 |
| Labeler Name: | STAT Rx USA LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA013217 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20071101 |
Package Information of METAXALONE
| Package NDC: | 16590-346-40 |
| Package Description: | 40 TABLET in 1 BOTTLE (16590-346-40) |
NDC Information of METAXALONE
| NDC Code | 16590-346-40 |
| Proprietary Name | METAXALONE |
| Package Description | 40 TABLET in 1 BOTTLE (16590-346-40) |
| Product NDC | 16590-346 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | METAXALONE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20071101 |
| Marketing Category Name | NDA |
| Labeler Name | STAT Rx USA LLC |
| Substance Name | METAXALONE |
| Strength Number | 800 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC] |
