Sertraline Hydrochloride
- Product NDC
- 35356-669
- 11-digit product format
- 353560669
- Labeler code
- 35356
- Product ID
- 35356-669_9086a9f5-b423-4e50-a9e3-485ba2f9c19b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sertraline Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
- Application
- ANDA077397
- Marketing category
- ANDA
- Marketing start
- 2007-12-18
- Marketing end
- 0000-00-00
- Substance
- SERTRALINE HYDROCHLORIDE
- Active strength
- 25 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