Methocarbamol
- Product NDC
- 68071-4458
- 11-digit product format
- 680714458
- Labeler code
- 68071
- Product ID
- 68071-4458_6d872d45-decc-74a4-e053-2a91aa0aaa80
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA085159
- Marketing category
- ANDA
- Marketing start
- 2000-01-01
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record