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Naproxen

NDC 11534-211, Naproxen, tablet, delayed release, from Sunrise Pharmaceutical, Inc..

Product NDC
11534-211
Status
Listed
Labeler
Sunrise Pharmaceutical, Inc.
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA091432
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/11534-211 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • NAPROXEN375 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
11534-211-0111534021101100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (11534-211-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f2fb222a-b854-4e6f-9027-2e08aed24185

Use it

Look up 11534-211 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/11534-211 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 11534-211. 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.