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Naproxen Sodium

NDC 72789-543, Naproxen Sodium, tablet, film coated, from PD-Rx Pharmaceuticals, Inc..

Product NDC
72789-543
Status
Listed
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA074661
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72789-543 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • NAPROXEN SODIUM220 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
72789-543-147278905431414 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-543-14)
72789-543-287278905432828 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-543-28)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.

Use it

Look up 72789-543 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72789-543 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72789-543. 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.