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Paroxetine

NDC 72789-420, paroxetine hydrochloride hemihydrate, tablet, film coated, from PD-Rx Pharmaceuticals, Inc..

Product NDC
72789-420
Status
Listed
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203854
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72789-420 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PAROXETINE HYDROCHLORIDE HEMIHYDRATE40 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
72789-420-907278904209090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-420-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/65c81817-34d3-4c57-a4bf-fb10be98386d

Use it

Look up 72789-420 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72789-420 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72789-420. 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.