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Fluoxetine

NDC 70518-3554, Fluoxetine Hydrochloride, capsule, from REMEDYREPACK INC..

Product NDC
70518-3554
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204597
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3554 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FLUOXETINE HYDROCHLORIDE40 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
70518-3554-07051835540030 CAPSULE in 1 BLISTER PACK (70518-3554-0)
70518-3554-17051835540190 CAPSULE in 1 BOTTLE, PLASTIC (70518-3554-1)
70518-3554-27051835540230 CAPSULE in 1 BOTTLE, PLASTIC (70518-3554-2)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d121146e-7439-4169-a421-dab7b882b8aa

Use it

Look up 70518-3554 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3554 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-3554. 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.