Methocarbamol
- Product NDC
- 68071-5222
- 11-digit product format
- 680715222
- Labeler code
- 68071
- Product ID
- 68071-5222_d772b1ea-b271-cf6e-e053-2a95a90aad25
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA200958
- Marketing category
- ANDA
- Marketing start
- 2018-10-09
- 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
- 2023-12-31
- 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 |
|---|
| 68071-5222-6 | 68071522206 | 60 TABLET, COATED in 1 BOTTLE (68071-5222-6) | 2020-03-26 | 0000-00-00 | No | No | Current |