Methocarbamol
- Product NDC
- 72789-022
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA208507
- Marketing category
- ANDA
- Substance
- METHOCARBAMOL
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 72789-022-01 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-022-01) | 2019-10-24 | | No | Historical |
| 72789-022-82 | 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-022-82) | 2019-10-24 | | No | Historical |
| 72789-022-90 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-022-90) | 2023-09-12 | | No | Historical |
| 72789-022-93 | 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-022-93) | 2023-09-12 | | No | Historical |
| 72789-022-98 | 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-022-98) | 2023-09-12 | | No | Historical |