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Paroxetine

NDC 71209-094, Paroxetine, tablet, film coated, extended release, from Cadila Pharmaceuticals Limited.

Product NDC
71209-094
Status
Listed
Labeler
Cadila Pharmaceuticals Limited
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/71209-094 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PAROXETINE HYDROCHLORIDE HEMIHYDRATE12.5 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
71209-094-017120900940130 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71209-094-01)
71209-094-1071209009410500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71209-094-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5e43cdbd-2419-434b-96b9-920f02558d1c

Use it

Look up 71209-094 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71209-094 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71209-094. 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.