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Naproxen Sodium

NDC 24979-252, Naproxen Sodium, tablet, film coated, extended release, from Upsher-Smith Laboratories, LLC.

Product NDC
24979-252
Status
Listed
Labeler
Upsher-Smith Laboratories, LLC
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/24979-252 \
  -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
24979-252-0124979025201100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (24979-252-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/7c22a2d6-821c-4f83-aead-e756aed930e5

Use it

Look up 24979-252 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/24979-252 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 24979-252. 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.