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fluoxetine hydrochloride

NDC 72162-1494, fluoxetine hydrochloride, tablet, coated, from Bryant Ranch Prepack.

Product NDC
72162-1494
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
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72162-1494 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FLUOXETINE HYDROCHLORIDE10 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
72162-1494-172162149401100 TABLET, COATED in 1 BOTTLE, PLASTIC (72162-1494-1)
72162-1494-37216214940330 TABLET, COATED in 1 BOTTLE, PLASTIC (72162-1494-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d4043133-38de-4faa-bb76-8fafa5913844

Use it

Look up 72162-1494 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72162-1494 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72162-1494. 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.