METHOCARBAMOL
- Product NDC
- 70934-322
- 11-digit product format
- 709340322
- Labeler code
- 70934
- Product ID
- 70934-322_b7b199ac-dec4-233c-e053-2a95a90a429a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METHOCARBAMOL
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA203550
- Marketing category
- ANDA
- Marketing start
- 2019-03-20
- 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
- 2021-12-31
- 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 |
|---|
| 70934-322-40 | 70934032240 | 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-322-40) | 2019-03-20 | 0000-00-00 | No | No | Current |