Fluoxetine hydrochloride
NDC 55111-284, Fluoxetine Hydrochloride, capsule, delayed release pellets, from Dr.Reddy's Laboratories Limited.
- Product NDC
- 55111-284
- Status
- Listed
- Labeler
- Dr.Reddy's Laboratories Limited
- Dosage form
- CAPSULE, DELAYED RELEASE PELLETS
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA078572
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/55111-284 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- FLUOXETINE HYDROCHLORIDE90 mg/1
Pharmacologic classes
Serotonin Reuptake Inhibitor [EPC]; Serotonin Uptake Inhibitors [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 55111-284-48 | 55111028448 | 1 BLISTER PACK in 1 CARTON (55111-284-48) / 4 CAPSULE, DELAYED RELEASE PELLETS in 1 BLISTER PACK |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/887fc670-db67-4cfe-967b-46b38375dae5NADAC price for package 55111028448
GET /v1/drugs/nadac/55111028448
Use it
Look up 55111-284 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/55111-284 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 55111-284. 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.