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Paroxetine Hydrochloride

NDC 62175-472, Paroxetine Hydrochloride, tablet, film coated, extended release, from Lannett Company, Inc..

Product NDC
62175-472
Status
Listed
Labeler
Lannett Company, Inc.
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204744
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/62175-472 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PAROXETINE HYDROCHLORIDE37.5 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
62175-472-326217504723230 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62175-472-32)
62175-472-4162175047241500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62175-472-41)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f22886f5-230c-47e4-9dd8-ffb14c8d6ae4

  • NADAC price for package 62175047232

    GET /v1/drugs/nadac/62175047232

Use it

Look up 62175-472 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/62175-472 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 62175-472. 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.