SERTRALINE HYDROCHLORIDE
- Product NDC
- 59762-4940
- 11-digit product format
- 597624940
- Labeler code
- 59762
- Product ID
- 59762-4940_9a484670-8be8-43ed-9ea9-a0567480993d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- sertraline hydrochloride
- Dosage form
- SOLUTION, CONCENTRATE
- Route
- ORAL
- Labeler
- Greenstone LLC
- Application
- NDA020990
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2006-03-20
- Marketing end
- 0000-00-00
- Substance
- SERTRALINE HYDROCHLORIDE
- Active strength
- 20 mg/mL
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA],Cytochrome P450 2D6 Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 59762-4940-1 | 59762494001 | 60 mL in 1 BOTTLE, DROPPER (59762-4940-1) | 60 ml | 2006-03-20 | 0000-00-00 | No | No | Current |