Methocarbamol
- Product NDC
- 70934-528
- 11-digit product format
- 709340528
- Labeler code
- 70934
- Product ID
- 70934-528_a9671e6c-2e78-28b5-e053-2995a90ae3a7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA085159
- Marketing category
- ANDA
- Marketing start
- 2020-01-28
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-528-20 | 70934052820 | 20 TABLET in 1 BOTTLE, PLASTIC (70934-528-20) | 20 tablet | 2020-05-11 | 0000-00-00 | No | No | Current |
| 70934-528-30 | 70934052830 | 30 TABLET in 1 BOTTLE, PLASTIC (70934-528-30) | 30 tablet | 2020-01-28 | 0000-00-00 | No | No | Current |
| 70934-528-40 | 70934052840 | 40 TABLET in 1 BOTTLE, PLASTIC (70934-528-40) | 40 tablet | 2020-03-12 | 0000-00-00 | No | No | Current |