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Paroxetine

NDC 72241-031, Paroxetine, tablet, film coated, extended release, from Modavar Pharmaceuticals LLC.

Product NDC
72241-031
Status
Listed
Labeler
Modavar Pharmaceuticals LLC
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA212645
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72241-031 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PAROXETINE HYDROCHLORIDE HEMIHYDRATE37.5 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
72241-031-1072241003110500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72241-031-10)
72241-031-227224100312230 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72241-031-22)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/555cfa31-3865-450f-b16b-2f4004af7a67

  • NADAC price for package 72241003122

    GET /v1/drugs/nadac/72241003122

Use it

Look up 72241-031 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72241-031 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72241-031. 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.