Fluoxetine
NDC 84386-104, Fluoxetine, tablet, film coated, from Aurobindo Pharma Limited.
- Product NDC
- 84386-104
- Status
- Listed
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA213286
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/84386-104 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- FLUOXETINE HYDROCHLORIDE10 mg/1
Pharmacologic classes
Serotonin Reuptake Inhibitor [EPC]; Serotonin Uptake Inhibitors [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 84386-104-01 | 84386010401 | 100 TABLET, FILM COATED in 1 BOTTLE (84386-104-01) |
| 84386-104-30 | 84386010430 | 30 TABLET, FILM COATED in 1 BOTTLE (84386-104-30) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/09fb3100-1e06-4cdc-8016-7e4f5d097490
Use it
Look up 84386-104 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/84386-104 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 84386-104. 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.