Paroxetine
NDC 70518-2574, Paroxetine, tablet, film coated, from REMEDYREPACK INC..
- Product NDC
- 70518-2574
- Status
- Listed
- Labeler
- REMEDYREPACK INC.
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA078406
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70518-2574 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- PAROXETINE HYDROCHLORIDE HEMIHYDRATE10 mg/1
Pharmacologic classes
Serotonin Reuptake Inhibitor [EPC]; Serotonin Uptake Inhibitors [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 70518-2574-4 | 70518257404 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2574-4) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/f52ca1fc-fbf7-4b2b-9e74-975c310b8ce6
Use it
Look up 70518-2574 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70518-2574 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70518-2574. 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.