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SKELAXIN
SKELAXIN - 60793-136-01 - (metaxalone)
Drug Information of SKELAXIN
| Product NDC: | 60793-136 |
| 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: | 60793-136 |
| Labeler Name: | King Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA013217 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20020830 |
Package Information of SKELAXIN
| Package NDC: | 60793-136-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (60793-136-01) |
NDC Information of SKELAXIN
| NDC Code | 60793-136-01 |
| Proprietary Name | SKELAXIN |
| Package Description | 100 TABLET in 1 BOTTLE (60793-136-01) |
| Product NDC | 60793-136 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | metaxalone |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20020830 |
| Marketing Category Name | NDA |
| Labeler Name | King Pharmaceuticals, Inc. |
| Substance Name | METAXALONE |
| Strength Number | 800 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC] |
