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Fluoxetine

NDC 54838-523, Fluoxetine Hydrochloride, liquid, from Lannett Company, Inc..

Product NDC
54838-523
Status
Listed
Labeler
Lannett Company, Inc.
Dosage form
LIQUID
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077849
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/54838-523 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FLUOXETINE HYDROCHLORIDE20 mg/5mL

Pharmacologic classes

Serotonin Reuptake Inhibitor [EPC]; Serotonin Uptake Inhibitors [MoA]

Package NDCNDC-11Package
54838-523-4054838052340120 mL in 1 BOTTLE, PLASTIC (54838-523-40)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c856d72f-4a1a-4f75-ae54-c4ac83ddcfa1

  • NADAC price for package 54838052340

    GET /v1/drugs/nadac/54838052340

Use it

Look up 54838-523 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/54838-523 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 54838-523. 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.