Methocarbamol Tablets, USP, 750 mg 750 mg/1
Methocarbamol · TABLET, FILM COATED · Granulation Technology, Inc.
Methocarbamol Tablets, USP, 750 mg is a tablet, film coated containing methocarbamol at 750 mg/1, taken oral. Manufactured by Granulation Technology, Inc..
Key Facts
- Brand Name
- Methocarbamol Tablets, USP, 750 mg
- Generic Name
- Methocarbamol
- NDC Code (Product)
63561-0174- Manufacturer
- Granulation Technology, Inc.
- Strength
- 750 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- ANDA212623
- Drug Class
- Muscle Relaxant [EPC]
- Marketing Start
- 06/10/2025
Recall History
No Recall HistoryFrequently Asked Questions
What is Methocarbamol Tablets, USP, 750 mg used for?
Methocarbamol Tablets, USP, 750 mg contains Methocarbamol. It is a tablet, film coated taken oral. Consult your doctor for specific uses.
Is Methocarbamol Tablets, USP, 750 mg a controlled substance?
Methocarbamol Tablets, USP, 750 mg is not classified as a controlled substance by the DEA.
What is the generic name for Methocarbamol Tablets, USP, 750 mg?
The generic name for Methocarbamol Tablets, USP, 750 mg is Methocarbamol. There are 12 other brand versions of Methocarbamol.
What is the NDC code for Methocarbamol Tablets, USP, 750 mg 750 mg/1?
The NDC (National Drug Code) for Methocarbamol Tablets, USP, 750 mg 750 mg/1 is 63561-0174, listed by Granulation Technology, 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.
Data from openFDA · Public domain (CC0 1.0)