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Fluoxetine

NDC 84386-106, Fluoxetine, tablet, film coated, from Aurobindo Pharma Limited.

Product NDC
84386-106
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213265
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/84386-106 \
  -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
84386-106-308438601063030 TABLET, FILM COATED in 1 BOTTLE (84386-106-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a9ed97dd-8041-4a02-889c-dcb8b2805f36

Use it

Look up 84386-106 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/84386-106 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 84386-106. 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.