SUNOSI
- Product NDC
- 68727-351
- 11-digit product format
- 687270351
- Labeler code
- 68727
- Product ID
- 68727-351_81387972-eb98-4943-a04e-4b8a727e23bf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- solriamfetol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Jazz Pharmaceuticals, Inc.
- Application
- NDA211230
- Marketing category
- NDA
- Marketing start
- 2019-06-18
- Marketing end
- 2025-10-31
- Substance
- SOLRIAMFETOL
- Active strength
- 150 mg/1
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68727-351-01 | 68727035101 | 30 TABLET, FILM COATED in 1 BOTTLE (68727-351-01) | 2019-06-18 | 2025-10-31 | No | No | Current |
| 68727-351-02 | 68727035102 | 100 TABLET, FILM COATED in 1 BOTTLE (68727-351-02) | 2019-06-18 | 2025-10-31 | No | No | Current |
| 68727-351-07 | 68727035107 | 7 TABLET, FILM COATED in 1 BLISTER PACK (68727-351-07) | 2019-06-18 | 2025-10-31 | No | No | Current |
| 68727-351-10 | 68727035110 | 10 TABLET, FILM COATED in 1 CARTON (68727-351-10) | 2019-06-18 | 2025-10-31 | No | No | Current |