Carisoprodol
- Product NDC
- 16714-510
- 11-digit product format
- 167140510
- Labeler code
- 16714
- Product ID
- 16714-510_98503121-ca36-e564-e053-2995a90a96aa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Carisoprodol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NorthStar RxLLC
- Application
- ANDA205085
- Marketing category
- ANDA
- Marketing start
- 2017-05-01
- 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
DailyMed Product Concepts#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 16714-510-01 | 16714051001 | 100 TABLET in 1 BOTTLE (16714-510-01) | 100 tablet | 2017-05-01 | 0000-00-00 | No | No | Current |
| 16714-510-02 | 16714051002 | 500 TABLET in 1 BOTTLE (16714-510-02) | 500 tablet | 2017-05-01 | 0000-00-00 | No | No | Current |
| 16714-510-03 | 16714051003 | 1000 TABLET in 1 BOTTLE (16714-510-03) | 1000 tablet | 2017-05-01 | 0000-00-00 | No | No | Current |