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Fluoxetine

NDC 0121-0721, FLUOXETINE HYDROCHLORIDE, solution, from PAI Holdings, LLC dba PAI Pharma.

Product NDC
0121-0721
Status
Listed
Labeler
PAI Holdings, LLC dba PAI Pharma
Dosage form
SOLUTION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA076015
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0121-0721 \
  -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
0121-0721-0400121072104120 mL in 1 BOTTLE (0121-0721-04)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/180a07fd-1f6a-4617-b8e0-f938c65ba273

Use it

Look up 0121-0721 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0121-0721 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0121-0721. 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.