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Fluoxetine

NDC 71209-041, Fluoxetine, capsule, from Cadila Pharmaceuticals Limited.

Product NDC
71209-041
Status
Listed
Labeler
Cadila Pharmaceuticals Limited
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA206993
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71209-041 \
  -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
71209-041-017120900410130 CAPSULE in 1 BOTTLE (71209-041-01)
71209-041-0571209004105100 CAPSULE in 1 BOTTLE (71209-041-05)
71209-041-1071209004110500 CAPSULE in 1 BOTTLE (71209-041-10)
71209-041-11712090041111000 CAPSULE in 1 BOTTLE (71209-041-11)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/9651816f-58f5-4bf8-8183-6f3d84d36b5c

Use it

Look up 71209-041 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71209-041 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71209-041. 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.