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Fluoxetine

NDC 49483-702, Fluoxetine Hydrochloride, capsule, from TIME CAP LABORATORIES, INC..

Product NDC
49483-702
Status
Listed
Labeler
TIME CAP LABORATORIES, INC.
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075465
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/49483-702 \
  -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
49483-702-0149483070201100 CAPSULE in 1 BOTTLE (49483-702-01)
49483-702-10494830702101000 CAPSULE in 1 BOTTLE (49483-702-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d7a4db7f-cdac-2b36-e053-2995a90a8d64

  • NADAC price for package 49483070201

    GET /v1/drugs/nadac/49483070201

  • NADAC price for package 49483070210

    GET /v1/drugs/nadac/49483070210

Use it

Look up 49483-702 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/49483-702 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 49483-702. 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.