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ROBAXIN
ROBAXIN - 0641-6103-25 - (methocarbamol)
Drug Information of ROBAXIN
| Product NDC: | 0641-6103 |
| Proprietary Name: | ROBAXIN |
| Non Proprietary Name: | methocarbamol |
| Active Ingredient(s): | 100 mg/mL & nbsp; methocarbamol |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ROBAXIN
| Product NDC: | 0641-6103 |
| Labeler Name: | West-ward Pharmaceutical Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA011790 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19590616 |
Package Information of ROBAXIN
| Package NDC: | 0641-6103-25 |
| Package Description: | 25 VIAL in 1 CARTON (0641-6103-25) > 10 mL in 1 VIAL (0641-6103-01) |
NDC Information of ROBAXIN
| NDC Code | 0641-6103-25 |
| Proprietary Name | ROBAXIN |
| Package Description | 25 VIAL in 1 CARTON (0641-6103-25) > 10 mL in 1 VIAL (0641-6103-01) |
| Product NDC | 0641-6103 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | methocarbamol |
| Dosage Form Name | INJECTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 19590616 |
| Marketing Category Name | NDA |
| Labeler Name | West-ward Pharmaceutical Corp. |
| Substance Name | METHOCARBAMOL |
| Strength Number | 100 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC] |
