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Sumatriptan and Naproxen Sodium

NDC 65862-928, Sumatriptan and Naproxen Sodium, tablet, film coated, from Aurobindo Pharma Limited.

Product NDC
65862-928
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA207457
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65862-928 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SUMATRIPTAN SUCCINATE85 mg/1
  • NAPROXEN SODIUM500 mg/1

Pharmacologic classes

Anti-Inflammatory Agents, Non-Steroidal [CS]; Cyclooxygenase Inhibitors [MoA]; Nonsteroidal Anti-inflammatory Drug [EPC]; Serotonin 1b Receptor Agonists [MoA]; Serotonin 1d Receptor Agonists [MoA]; Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]

Package NDCNDC-11Package
65862-928-36658620928369 TABLET, FILM COATED in 1 BOTTLE (65862-928-36)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f5203c66-0a40-4263-a237-b71e930e4697
  • NADAC price for package 65862092836

    GET /v1/drugs/nadac/65862092836

Use it

Look up 65862-928 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65862-928 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65862-928. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.