Sertraline Hydrochloride
- Product NDC
- 50090-1847
- 11-digit product format
- 500901847
- Labeler code
- 50090
- Product ID
- 50090-1847_995d7dc0-ef3d-418a-9ff6-6b463a6740f2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sertraline Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA077206
- Marketing category
- ANDA
- Marketing start
- 2007-02-06
- Marketing end
- 0000-00-00
- Substance
- SERTRALINE HYDROCHLORIDE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 50090-1847-1 | 50090184701 | 60 TABLET, FILM COATED in 1 BOTTLE (50090-1847-1) | 2015-05-27 | 0000-00-00 | No | No | Current |
| 50090-1847-2 | 50090184702 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-1847-2) | 2015-05-27 | 0000-00-00 | No | No | Current |