SERTRALINE HYDROCHLORIDE
- Product NDC
- 35356-832
- 11-digit product format
- 353560832
- Labeler code
- 35356
- Product ID
- 35356-832_fe06b0b9-9e79-41bd-b9a1-ffe80d078b6a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SERTRALINE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA077670
- Marketing category
- ANDA
- Marketing start
- 2007-01-02
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record