Paroxetine
NDC 72189-492, Paroxetine, tablet, film coated, from Direct_Rx.
- Product NDC
- 72189-492
- Status
- Listed
- Labeler
- Direct_Rx
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA077584
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/72189-492 \ -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 |
|---|---|---|
| 72189-492-30 | 72189049230 | 30 TABLET, FILM COATED in 1 BOTTLE (72189-492-30) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/fea936a5-fdeb-e4fb-e053-6294a90a8995
Use it
Look up 72189-492 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/72189-492 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 72189-492. 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.