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ROBAXIN
ROBAXIN - 16590-981-72 - (METHOCARBAMOL)
Drug Information of ROBAXIN
| Product NDC: | 16590-981 |
| Proprietary Name: | ROBAXIN |
| Non Proprietary Name: | METHOCARBAMOL |
| Active Ingredient(s): | 750 mg/1 & nbsp; METHOCARBAMOL |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ROBAXIN
| Product NDC: | 16590-981 |
| Labeler Name: | STAT RX USA LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA011011 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20030120 |
Package Information of ROBAXIN
| Package NDC: | 16590-981-72 |
| Package Description: | 120 TABLET, FILM COATED in 1 BOTTLE (16590-981-72) |
NDC Information of ROBAXIN
| NDC Code | 16590-981-72 |
| Proprietary Name | ROBAXIN |
| Package Description | 120 TABLET, FILM COATED in 1 BOTTLE (16590-981-72) |
| Product NDC | 16590-981 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | METHOCARBAMOL |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20030120 |
| Marketing Category Name | NDA |
| Labeler Name | STAT RX USA LLC |
| Substance Name | METHOCARBAMOL |
| Strength Number | 750 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC] |
