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Fluoxetine Hydrochloride

NDC 70954-600, Fluoxetine Hydrochloride, solution, from ANI Pharmaceuticals, Inc..

Product NDC
70954-600
Status
Listed
Labeler
ANI Pharmaceuticals, Inc.
Dosage form
SOLUTION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA216448
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70954-600 \
  -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
70954-600-1070954060010120 mL in 1 BOTTLE, PLASTIC (70954-600-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1ffe57c3-6f70-4075-aacb-d87a3990fdea

  • NADAC price for package 70954060010

    GET /v1/drugs/nadac/70954060010

Use it

Look up 70954-600 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70954-600 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70954-600. 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.