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Naproxen

NDC 69097-852, Naproxen, tablet, delayed release, from Cipla USA Inc..

Product NDC
69097-852
Status
Listed
Labeler
Cipla USA 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/69097-852 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • NAPROXEN500 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
69097-852-0769097085207100 TABLET, DELAYED RELEASE in 1 BOTTLE (69097-852-07)
69097-852-1269097085212500 TABLET, DELAYED RELEASE in 1 BOTTLE (69097-852-12)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e06c2b43-9882-442e-8413-10d9a33aecb9

Use it

Look up 69097-852 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69097-852 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69097-852. 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.