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Paroxetine

NDC 55289-037, paroxetine hydrochloride hemihydrate, tablet, film coated, from PD-Rx Pharmaceuticals, Inc..

Product NDC
55289-037
Status
Listed
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078902
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/55289-037 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PAROXETINE HYDROCHLORIDE10 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
55289-037-455528900374545 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-037-45)
55289-037-905528900379090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-037-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ff7c7e20-c9ee-4693-beaa-7ac532d5c4b7

Use it

Look up 55289-037 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/55289-037 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 55289-037. 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.