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Fluoxetine

NDC 42708-200, Fluoxetine, capsule, from QPharma Inc.

Product NDC
42708-200
Status
Listed
Labeler
QPharma Inc
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078619
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/42708-200 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FLUOXETINE HYDROCHLORIDE20 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
42708-200-304270802003030 CAPSULE in 1 BOTTLE, PLASTIC (42708-200-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/50253c6e-de36-05e6-e063-6294a90ad7a8

Use it

Look up 42708-200 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/42708-200 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 42708-200. 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.