Carisoprodol
- Product NDC
- 70518-1401
- 11-digit product format
- 705181401
- Labeler code
- 70518
- Product ID
- 70518-1401_92bc6ead-aeb4-2f26-e053-2995a90aaed5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Carisoprodol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA087499
- Marketing category
- ANDA
- Marketing start
- 2018-09-06
- 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