Methocarbamol
- Product NDC
- 55700-716
- 11-digit product format
- 557000716
- Labeler code
- 55700
- Product ID
- 55700-716_91874264-27d5-43d1-8074-ce4b6d1965b6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA208507
- Marketing category
- ANDA
- Marketing start
- 2018-01-15
- Marketing end
- 0000-00-00
- Substance
- METHOCARBAMOL
- Active strength
- 500 mg/1
- Pharmacologic classes
- Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-716-01 | 55700071601 | 120 TABLET, FILM COATED in 1 BOTTLE (55700-716-01) | 2019-02-08 | 0000-00-00 | No | No | Current |
| 55700-716-20 | 55700071620 | 20 TABLET, FILM COATED in 1 BOTTLE (55700-716-20) | 2019-01-11 | 0000-00-00 | No | No | Current |
| 55700-716-30 | 55700071630 | 30 TABLET, FILM COATED in 1 BOTTLE (55700-716-30) | 2019-01-11 | 0000-00-00 | No | No | Current |
| 55700-716-60 | 55700071660 | 60 TABLET, FILM COATED in 1 BOTTLE (55700-716-60) | 2019-01-11 | 0000-00-00 | No | No | Current |
| 55700-716-90 | 55700071690 | 90 TABLET, FILM COATED in 1 BOTTLE (55700-716-90) | 2019-01-11 | 0000-00-00 | No | No | Current |