Methocarbamol
- Product NDC
- 70518-4501
- 11-digit product format
- 705184501
- Labeler code
- 70518
- Product ID
- 70518-4501_410c526a-4b20-423b-e063-6294a90ac9fe
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol Tablets
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA209312
- Marketing category
- ANDA
- Marketing start
- 2025-10-13
- Substance
- METHOCARBAMOL
- Active strength
- 750 mg/1
- Pharmacologic classes
- Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 125OD7737X | METHOCARBAMOL | 532-03-6 | METHOCARBAMOL |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 70518-4501-0 | 70518450100 | 40 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-4501-0) | 2025-10-13 | No | No | Historical |