Methocarbamol
- Product NDC
- 71205-103
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA208507
- Marketing category
- ANDA
- Substance
- METHOCARBAMOL
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 71205-103-20 | 20 TABLET, FILM COATED in 1 BOTTLE (71205-103-20) | 2018-09-04 | | No | Historical |
| 71205-103-30 | 30 TABLET, FILM COATED in 1 BOTTLE (71205-103-30) | 2018-09-04 | | No | Historical |
| 71205-103-40 | 40 TABLET, FILM COATED in 1 BOTTLE (71205-103-40) | 2018-09-04 | | No | Historical |
| 71205-103-45 | 45 TABLET, FILM COATED in 1 BOTTLE (71205-103-45) | 2018-09-04 | | No | Historical |
| 71205-103-60 | 60 TABLET, FILM COATED in 1 BOTTLE (71205-103-60) | 2018-09-04 | | No | Historical |
| 71205-103-90 | 90 TABLET, FILM COATED in 1 BOTTLE (71205-103-90) | 2018-09-04 | | No | Historical |