SERTRALINE HYDROCHLORIDE
- Product NDC
- 68788-7001
- 11-digit product format
- 687887001
- Labeler code
- 68788
- Product ID
- 68788-7001_29636aac-47e1-4a65-9891-91904dedc51d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SERTRALINE HYDROCHLORIDE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA202825
- Marketing category
- ANDA
- Marketing start
- 2017-08-07
- Marketing end
- 0000-00-00
- Substance
- SERTRALINE HYDROCHLORIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record