Sertraline Hydrochloride
NDC 42708-124, Sertraline Hydrochloride, tablet, film coated, from QPharma Inc.
- Product NDC
- 42708-124
- Status
- Listed
- Labeler
- QPharma Inc
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA077206
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/42708-124 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SERTRALINE HYDROCHLORIDE50 mg/1
Pharmacologic classes
Cytochrome P450 2D6 Inhibitors [MoA]; Serotonin Reuptake Inhibitor [EPC]; Serotonin Uptake Inhibitors [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 42708-124-30 | 42708012430 | 30 TABLET, FILM COATED in 1 BOTTLE (42708-124-30) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/664d1744-7b1d-43e2-98ba-1b0e69d75840
Use it
Look up 42708-124 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/42708-124 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 42708-124. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.