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FLUOXETINE

NDC 71656-089, FLUOXETINE, solution, from Saptalis Pharmaceuticals, LLC..

Product NDC
71656-089
Status
Listed
Labeler
Saptalis Pharmaceuticals, LLC.
Dosage form
SOLUTION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075525
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71656-089 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FLUOXETINE HYDROCHLORIDE20 mg/5mL

Pharmacologic classes

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

Package NDCNDC-11Package
71656-089-0471656008904120 mL in 1 BOTTLE (71656-089-04)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4527c502-b28c-449f-ad2d-7daf21563cfa

  • NADAC price for package 71656008904

    GET /v1/drugs/nadac/71656008904

Use it

Look up 71656-089 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71656-089 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71656-089. 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.