fluoxetine hydrochloride
NDC 63629-2200, fluoxetine hydrochloride, tablet, coated, from Bryant Ranch Prepack.
- Product NDC
- 63629-2200
- Status
- Listed
- Labeler
- Bryant Ranch Prepack
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA203836
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/63629-2200 \ -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 |
|---|---|---|
| 63629-2200-1 | 63629220001 | 100 TABLET, COATED in 1 BOTTLE, PLASTIC (63629-2200-1) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/72e391aa-1a46-4589-8550-f83ac9241cf1
Use it
Look up 63629-2200 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/63629-2200 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 63629-2200. 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.