Sertraline Hydrochloride
- Product NDC
- 63739-490
- 11-digit product format
- 637390490
- Labeler code
- 63739
- Product ID
- 63739-490_e6d920ee-80bc-4247-8b50-77f463130d38
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sertraline Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- McKesson Packaging Services Business Unit of McKesson Corporation
- Application
- ANDA077206
- Marketing category
- ANDA
- Marketing start
- 2010-12-01
- 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
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#