Methocarbamol Tablets, USP, 500 mg
- Product NDC
- 72789-499
- 11-digit product format
- 727890499
- Labeler code
- 72789
- Product ID
- 72789-499_396bde13-ddeb-7ed6-e063-6294a90abdd7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA212623
- Marketing category
- ANDA
- Marketing start
- 2024-01-01
- Substance
- METHOCARBAMOL
- Active strength
- 500 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 |
|---|
| 72789-499-18 | 72789049918 | 18 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-499-18) | 2025-04-16 | No | No | Historical |
| 72789-499-20 | 72789049920 | 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-499-20) | 2025-04-28 | No | No | Historical |
| 72789-499-28 | 72789049928 | 28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-499-28) | 2025-07-08 | No | No | Historical |