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Fluoxetine

NDC 16714-112, Fluoxetine, tablet, film coated, from NorthStar Rx LLC.

Product NDC
16714-112
Status
Listed
Labeler
NorthStar Rx LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA076006
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/16714-112 \
  -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
16714-112-011671401120130 TABLET, FILM COATED in 1 BOTTLE (16714-112-01)
16714-112-0216714011202100 TABLET, FILM COATED in 1 BOTTLE (16714-112-02)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/70b4bd1b-d355-189e-a414-9fff182fd1cd

  • NADAC price for package 16714011201

    GET /v1/drugs/nadac/16714011201

  • NADAC price for package 16714011202

    GET /v1/drugs/nadac/16714011202

Use it

Look up 16714-112 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/16714-112 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 16714-112. 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.