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Fluoxetine

NDC 71205-393, Fluoxetine Hydrochloride, capsule, from Proficient Rx LP.

Product NDC
71205-393
Status
Listed
Labeler
Proficient Rx LP
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/71205-393 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FLUOXETINE HYDROCHLORIDE40 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
71205-393-307120503933030 CAPSULE in 1 BOTTLE (71205-393-30)
71205-393-607120503936060 CAPSULE in 1 BOTTLE (71205-393-60)
71205-393-907120503939090 CAPSULE in 1 BOTTLE (71205-393-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ef699ed0-fd9e-4580-93bb-6fd50499dbd1

Use it

Look up 71205-393 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-393 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-393. 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.