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fluoxetine hydrochloride

NDC 63629-8990, fluoxetine hydrochloride, tablet, coated, from Bryant Ranch Prepack.

Product NDC
63629-8990
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
TABLET, COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203836
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/63629-8990 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FLUOXETINE HYDROCHLORIDE20 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
63629-8990-16362989900160 TABLET, COATED in 1 BOTTLE, PLASTIC (63629-8990-1)
63629-8990-26362989900290 TABLET, COATED in 1 BOTTLE, PLASTIC (63629-8990-2)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/da785a8a-d897-494e-9fd2-1d09b32f0190

Use it

Look up 63629-8990 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/63629-8990 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 63629-8990. 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.