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Fluoxetine

NDC 50228-422, FLUOXETINE HYDROCHLORIDE, tablet, from ScieGen Pharmaceuticals, Inc..

Product NDC
50228-422
Status
Listed
Labeler
ScieGen Pharmaceuticals, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA211282
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50228-422 \
  -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 NDCNDC-11Package
50228-422-10502280422101000 TABLET in 1 BOTTLE (50228-422-10)
50228-422-305022804223030 TABLET in 1 BOTTLE (50228-422-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a7ba9184-7dad-4f82-a947-bb2cc6b760ce

  • NADAC price for package 50228042230

    GET /v1/drugs/nadac/50228042230

Use it

Look up 50228-422 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50228-422 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50228-422. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.