carisoprodol
- Product NDC
- 70518-3792
- 11-digit product format
- 705183792
- Labeler code
- 70518
- Product ID
- 70518-3792_4c21828c-e4d7-305a-e063-6294a90a9c9a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- carisoprodol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA040792
- Marketing category
- ANDA
- Marketing start
- 2023-07-14
- 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
- 2027-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 21925K482H | CARISOPRODOL | 78-44-4 | CARISOPRODOL |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70518-3792-0 | 70518379200 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-3792-0) | 90 tablet | 2023-07-14 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| carisoprodol | REMEDYREPACK INC. | 2026-03-03 | HUMAN PRESCRIPTION DRUG LABEL | 6 |