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Sumatriptan and Naproxen Sodium

NDC 16714-891, Sumatriptan and Naproxen Sodium, tablet, film coated, from NorthStar RxLLC.

Product NDC
16714-891
Status
Listed
Labeler
NorthStar RxLLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202803
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/16714-891 \
  -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
16714-891-01167140891019 TABLET, FILM COATED in 1 BOTTLE (16714-891-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3f2ec27e-0e96-4028-a1fa-114e6d501464

  • NADAC price for package 16714089101

    GET /v1/drugs/nadac/16714089101

Use it

Look up 16714-891 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/16714-891 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 16714-891. 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.