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Fluoxetine hydrochloride

NDC 16714-114, Fluoxetine hydrochloride, tablet, film coated, from NorthStar Rx LLC.

Product NDC
16714-114
Status
Listed
Labeler
NorthStar Rx LLC
Dosage form
TABLET, FILM COATED
Route
ORAL, ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA211721
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/16714-114 \
  -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
16714-114-011671401140130 TABLET, FILM COATED in 1 BOTTLE (16714-114-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1f8b1834-d5d7-72b6-d2ed-cb074344d59e

  • NADAC price for package 16714011401

    GET /v1/drugs/nadac/16714011401

Use it

Look up 16714-114 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/16714-114 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 16714-114. 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.