Carisoprodol
- Product NDC
- 71335-2708
- 11-digit product format
- 713352708
- Labeler code
- 71335
- Product ID
- 71335-2708_7d96e012-f690-452d-a0b0-1c8da2ec2f9a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Carisoprodol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA207237
- Marketing category
- ANDA
- Marketing start
- 2017-05-12
- Substance
- CARISOPRODOL
- Active strength
- 250 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Carisoprodol
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CARISOPRODOL | 250 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 21925K482H |
| Rxcui | 730794 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71335-2708-1 | Carisoprodol | 100 in 1 BOTTLE | TABLET | 100 | | 100 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2708-1 | 71335270801 | 100 TABLET in 1 BOTTLE (71335-2708-1) | 100 tablet | 2025-07-28 | No | No | Current |