Fluoxetine
NDC 82009-101, Fluoxetine Hydrochloride, capsule, from QUALLENT PHARMACEUTICALS HEALTH LLC.
- Product NDC
- 82009-101
- Status
- Listed
- Labeler
- QUALLENT PHARMACEUTICALS HEALTH LLC
- Dosage form
- CAPSULE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA078619
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/82009-101 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- FLUOXETINE HYDROCHLORIDE20 mg/1
Pharmacologic classes
Serotonin Reuptake Inhibitor [EPC]; Serotonin Uptake Inhibitors [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 82009-101-10 | 82009010110 | 1000 CAPSULE in 1 BOTTLE (82009-101-10) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/4abbd9d9-e9b1-463d-8f39-f3f50d80f58aNADAC price for package 82009010110
GET /v1/drugs/nadac/82009010110
Use it
Look up 82009-101 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/82009-101 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 82009-101. 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.