Methocarbamol
- Product NDC
- 55700-720
- 11-digit product format
- 557000720
- Labeler code
- 55700
- Product ID
- 55700-720_9579fdb7-47f3-4242-b627-780fcea4222b
- 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
- 2019-01-18
- 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
- 2022-12-31
- 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 |
|---|
| 55700-720-01 | 55700072001 | 120 TABLET, FILM COATED in 1 BOTTLE (55700-720-01) | 2019-01-18 | 0000-00-00 | No | No | Current |
| 55700-720-30 | 55700072030 | 30 TABLET, FILM COATED in 1 BOTTLE (55700-720-30) | 2019-01-18 | 0000-00-00 | No | No | Current |
| 55700-720-40 | 55700072040 | 40 TABLET, FILM COATED in 1 BOTTLE (55700-720-40) | 2019-01-18 | 0000-00-00 | No | No | Current |
| 55700-720-60 | 55700072060 | 60 TABLET, FILM COATED in 1 BOTTLE (55700-720-60) | 2019-01-18 | 0000-00-00 | No | No | Current |
| 55700-720-90 | 55700072090 | 90 TABLET, FILM COATED in 1 BOTTLE (55700-720-90) | 2019-01-18 | 0000-00-00 | No | No | Current |