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Naproxen Sodium

NDC 0480-0951, naproxen sodium, tablet, film coated, extended release, from Teva Pharmaceuticals, Inc..

Product NDC
0480-0951
Status
Listed
Labeler
Teva Pharmaceuticals, Inc.
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075416
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0480-0951 \
  -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
0480-0951-0100480095101100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0480-0951-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/826fd9e3-22fe-408b-820c-f2b710189555

Use it

Look up 0480-0951 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0480-0951 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0480-0951. 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.