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Fluoxetine

NDC 51655-750, Fluoxetine Hydrochloride, capsule, from Northwind Health Company, LLC.

Product NDC
51655-750
Status
Listed
Labeler
Northwind Health Company, LLC
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078619
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51655-750 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FLUOXETINE HYDROCHLORIDE10 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
51655-750-265165507502690 CAPSULE in 1 BOTTLE, PLASTIC (51655-750-26)
51655-750-525165507505230 CAPSULE in 1 BOTTLE, PLASTIC (51655-750-52)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/da6b9b19-2ea1-9a39-e053-2995a90ad730

Use it

Look up 51655-750 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51655-750 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51655-750. 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.