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Paroxetine

NDC 69367-335, Paroxetine, tablet, film coated, extended release, from Westminster Pharmaceuticals, LLC.

Product NDC
69367-335
Status
Listed
Labeler
Westminster Pharmaceuticals, LLC
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213485
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69367-335 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PAROXETINE HYDROCHLORIDE12.5 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
69367-335-306936703353030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (69367-335-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f39a2a7a-7a7e-4dd8-9704-54d9598504fb

  • NADAC price for package 69367033530

    GET /v1/drugs/nadac/69367033530

Use it

Look up 69367-335 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69367-335 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69367-335. 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.