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Naproxen Sodium

NDC 47781-153, Naproxen Sodium, tablet, film coated, extended release, from Alvogen Inc..

Product NDC
47781-153
Status
Listed
Labeler
Alvogen Inc.
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA AUTHORIZED GENERIC
Application
NDA020353
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/47781-153 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • NAPROXEN SODIUM375 mg/1

Pharmacologic classes

Anti-Inflammatory Agents, Non-Steroidal [CS]; Cyclooxygenase Inhibitors [MoA]; Nonsteroidal Anti-inflammatory Drug [EPC]

Package NDCNDC-11Package
47781-153-0147781015301100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47781-153-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/9225acaa-209f-958b-2c51-9a46995dec33

Use it

Look up 47781-153 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/47781-153 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 47781-153. 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.