Methocarbamol
- Product NDC
- 70518-2209
- 11-digit product format
- 705182209
- Labeler code
- 70518
- Product ID
- 70518-2209_daf9ff98-0392-f7e4-e053-2995a90a6373
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA208507
- Marketing category
- ANDA
- Marketing start
- 2019-07-11
- Marketing end
- 0000-00-00
- Substance
- METHOCARBAMOL
- Active strength
- 750 mg/1
- Pharmacologic classes
- Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2209-0 | 70518220900 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2209-0) | 2019-07-11 | 0000-00-00 | No | No | Current |
| 70518-2209-1 | 70518220901 | 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2209-1) | 2020-07-29 | 0000-00-00 | No | No | Current |