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NDC 79903-609, Naproxen sodium, tablet, coated, from Walmart Inc..

Product NDC
79903-609
Status
Listed
Labeler
Walmart Inc.
Dosage form
TABLET, COATED
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA090545
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/79903-609 \
  -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
79903-609-09799030609091 BOTTLE in 1 CARTON (79903-609-09) / 90 TABLET, COATED in 1 BOTTLE
79903-609-20799030609201 BOTTLE in 1 CARTON (79903-609-20) / 200 TABLET, COATED in 1 BOTTLE

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 79903-609 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/79903-609 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 79903-609. 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.