Paroxetine
NDC 71610-204, paroxetine hydrochloride hemihydrate, tablet, film coated, from Aphena Pharma Solutions - Tennessee, LLC.
- Product NDC
- 71610-204
- Status
- Listed
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA078902
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/71610-204 \ -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 |
|---|---|---|
| 71610-204-60 | 71610020460 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-204-60) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/2eebd2b6-7c64-45ca-8eb5-5201137f610a
Use it
Look up 71610-204 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71610-204 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71610-204. 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.