Methocarbamol Tablets, USP, 750 mg
- Product NDC
- 63561-0108
- 11-digit product format
- 635610108
- Labeler code
- 63561
- Product ID
- 63561-0108_c183bfe7-8c04-1096-e053-2a95a90ad512
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Granulation Technology, Inc.
- Application
- ANDA212623
- Marketing category
- ANDA
- Marketing start
- 2021-04-30
- 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 |
|---|
| 63561-0108-1 | 63561010801 | 100 TABLET, FILM COATED in 1 BOTTLE (63561-0108-1) | 2021-04-30 | 0000-00-00 | No | No | Current |
| 63561-0108-5 | 63561010805 | 500 TABLET, FILM COATED in 1 BOTTLE (63561-0108-5) | 2021-04-30 | 0000-00-00 | No | No | Current |