carisoprodol
- Product NDC
- 68071-3421
- 11-digit product format
- 680713421
- Labeler code
- 68071
- Product ID
- 68071-3421_2d584ea9-407f-a440-e063-6294a90a48cd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- carisoprodol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA040792
- Marketing category
- ANDA
- Marketing start
- 2009-08-06
- 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
- 2026-12-31
- 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 |
|---|
| 68071-3421-6 | 68071342106 | 60 TABLET in 1 BOTTLE (68071-3421-6) | 60 tablet | 2023-05-31 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| carisoprodol | NuCare Pharmaceuticals,Inc. | 2025-02-04 | HUMAN PRESCRIPTION DRUG LABEL | 2 |