Carisoprodol
- Product NDC
- 72789-019
- 11-digit product format
- 727890019
- Labeler code
- 72789
- Product ID
- 72789-019_e60ccd33-49fa-fa6b-e053-2a95a90a6ffb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Carisoprodol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA040245
- Marketing category
- ANDA
- Marketing start
- 2019-08-08
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72789-019-01 | 72789001901 | 100 TABLET in 1 BOTTLE, PLASTIC (72789-019-01) | 100 tablet | 2019-10-24 | 0000-00-00 | No | No | Current |
| 72789-019-90 | 72789001990 | 90 TABLET in 1 BOTTLE, PLASTIC (72789-019-90) | 90 tablet | 2019-10-24 | 0000-00-00 | No | No | Current |
| 72789-019-95 | 72789001995 | 1000 TABLET in 1 BOTTLE, PLASTIC (72789-019-95) | 1000 tablet | 2019-10-24 | 0000-00-00 | No | No | Current |
| 72789-019-98 | 72789001998 | 120 TABLET in 1 BOTTLE, PLASTIC (72789-019-98) | 120 tablet | 2019-10-24 | 0000-00-00 | No | No | Current |