Carisoprodol
- Product NDC
- 68071-4112
- 11-digit product format
- 680714112
- Labeler code
- 68071
- Product ID
- 68071-4112_5ae2ee9f-b4f2-e2bd-e053-2991aa0ab0e3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Carisoprodol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA087499
- Marketing category
- ANDA
- Marketing start
- 1987-11-01
- Marketing end
- 0000-00-00
- Substance
- CARISOPRODOL
- Active strength
- 350 mg/1
- Pharmacologic classes
- Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record