Methocarbamol Tablets, USP, 500 mg 500 mg/1
Methocarbamol · TABLET, FILM COATED · PD-Rx Pharmaceuticals, Inc.
Methocarbamol Tablets, USP, 500 mg is a tablet, film coated containing methocarbamol at 500 mg/1, taken oral. Manufactured by PD-Rx Pharmaceuticals, Inc..
Key Facts
- Brand Name
- Methocarbamol Tablets, USP, 500 mg
- Generic Name
- Methocarbamol
- NDC Code (Product)
72789-499- Manufacturer
- PD-Rx Pharmaceuticals, Inc.
- Strength
- 500 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- ANDA212623
- Drug Class
- Muscle Relaxant [EPC]
- Marketing Start
- 01/01/2024
Recall History
No Recall HistoryFrequently Asked Questions
What is Methocarbamol Tablets, USP, 500 mg used for?
Methocarbamol Tablets, USP, 500 mg contains Methocarbamol. It is a tablet, film coated taken oral. Consult your doctor for specific uses.
Is Methocarbamol Tablets, USP, 500 mg a controlled substance?
Methocarbamol Tablets, USP, 500 mg is not classified as a controlled substance by the DEA.
What is the generic name for Methocarbamol Tablets, USP, 500 mg?
The generic name for Methocarbamol Tablets, USP, 500 mg is Methocarbamol. There are 12 other brand versions of Methocarbamol.
What is the NDC code for Methocarbamol Tablets, USP, 500 mg 500 mg/1?
The NDC (National Drug Code) for Methocarbamol Tablets, USP, 500 mg 500 mg/1 is 72789-499, listed by PD-Rx Pharmaceuticals, Inc..
Other Methocarbamol Brands
See all →- Methocarbamol500 mg/172865-233
- methocarbamol1000 mg/172887-873
- Methocarbamol750 mg/180425-0490
- Methocarbamol500 mg/187063-040
- Methocarbamol500 mg/115014-910
- Methocarbamol500 mg/150090-0182
- METHOCARBAMOL500 mg/161919-368
- Methocarbamol500 mg/163629-1123
- Methocarbamol500 mg/167046-0538
- Methocarbamol500 mg/168071-3636
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
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