| NDC Code | 72789-521-60 |
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| Package Description | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-521-60) |
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| Product NDC | 72789-521 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Methocarbamol Tablets, Usp, 750 Mg |
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| Non-Proprietary Name | Methocarbamol |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20250610 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA212623 |
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| Manufacturer | PD-Rx Pharmaceuticals, Inc. |
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| Substance Name | METHOCARBAMOL |
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| Strength | 750 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC] |
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