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PAROXETINE

NDC 67544-492, paroxetine hydrochloride, tablet, film coated, from Aphena Pharma Solutions - Tennessee, LLC.

Product NDC
67544-492
Status
Listed
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075356
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/67544-492 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PAROXETINE HYDROCHLORIDE ANHYDROUS40 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
67544-492-156754404921515 TABLET, FILM COATED in 1 BOTTLE (67544-492-15)
67544-492-306754404923030 TABLET, FILM COATED in 1 BOTTLE (67544-492-30)
67544-492-456754404924545 TABLET, FILM COATED in 1 BOTTLE (67544-492-45)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a7128be7-7023-40c4-aa64-29d52145ae31

Use it

Look up 67544-492 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/67544-492 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 67544-492. 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.