Fluoxetine
NDC 49884-468, Fluoxetine, tablet, film coated, from Par Health USA, LLC.
- Product NDC
- 49884-468
- Status
- Listed
- Labeler
- Par Health USA, LLC
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA209419
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/49884-468 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- FLUOXETINE HYDROCHLORIDE60 mg/1
Pharmacologic classes
Serotonin Reuptake Inhibitor [EPC]; Serotonin Uptake Inhibitors [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 49884-468-11 | 49884046811 | 30 TABLET, FILM COATED in 1 BOTTLE (49884-468-11) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/6fff3732-efc3-4cbd-a8fa-cde3181f03e6NADAC price for package 49884046811
GET /v1/drugs/nadac/49884046811
Use it
Look up 49884-468 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/49884-468 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 49884-468. 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.