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FLUOXETINE HYDROCHLORIDE

NDC 51672-5306, FLUOXETINE HYDROCHLORIDE, tablet, film coated, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-5306
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA211477
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-5306 \
  -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
51672-5306-251672530602500 TABLET, FILM COATED in 1 BOTTLE (51672-5306-2)
51672-5306-65167253060630 TABLET, FILM COATED in 1 BOTTLE (51672-5306-6)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/77b6ae48-8e3a-42e6-9b5a-aeed750861e8

Use it

Look up 51672-5306 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-5306 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-5306. 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.