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fluoxetine hydrochloride

NDC 49884-335, fluoxetine hydrochloride, tablet, coated, from Par Health USA, LLC.

Product NDC
49884-335
Status
Listed
Labeler
Par Health USA, LLC
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/49884-335 \
  -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
49884-335-0149884033501100 TABLET, COATED in 1 BOTTLE, PLASTIC (49884-335-01)
49884-335-114988403351130 TABLET, COATED in 1 BOTTLE, PLASTIC (49884-335-11)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/53ac797d-8792-4a8c-9708-d1de3d377e8f

  • NADAC price for package 49884033501

    GET /v1/drugs/nadac/49884033501

  • NADAC price for package 49884033511

    GET /v1/drugs/nadac/49884033511

Use it

Look up 49884-335 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/49884-335 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 49884-335. 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.