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Fluoxetine

NDC 71205-125, Fluoxetine Hydrochloride, capsule, from Proficient Rx LP.

Product NDC
71205-125
Status
Listed
Labeler
Proficient Rx LP
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204597
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71205-125 \
  -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
71205-125-307120501253030 CAPSULE in 1 BOTTLE (71205-125-30)
71205-125-607120501256060 CAPSULE in 1 BOTTLE (71205-125-60)
71205-125-907120501259090 CAPSULE in 1 BOTTLE (71205-125-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0cba1992-3990-42a1-9d9a-77b593bbb02e

Use it

Look up 71205-125 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-125 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-125. 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.