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Naproxen Sodium

NDC 65862-515, Naproxen Sodium, tablet, film coated, from Aurobindo Pharma Limited.

Product NDC
65862-515
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA200629
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65862-515 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • NAPROXEN SODIUM275 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
65862-515-0165862051501100 TABLET, FILM COATED in 1 BOTTLE (65862-515-01)
65862-515-0565862051505500 TABLET, FILM COATED in 1 BOTTLE (65862-515-05)
65862-515-99658620515991000 TABLET, FILM COATED in 1 BOTTLE (65862-515-99)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/37b264f9-b46d-4635-8fab-246b1e08b653

  • NADAC price for package 65862051501

    GET /v1/drugs/nadac/65862051501

Use it

Look up 65862-515 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65862-515 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65862-515. 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.