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Naproxen Sodium

NDC 58602-738, Naproxen Sodium, tablet, film coated, from Aurohealth LLC.

Product NDC
58602-738
Status
Listed
Labeler
Aurohealth LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA205497
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/58602-738 \
  -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
58602-738-07586020738071 BOTTLE in 1 CARTON (58602-738-07) / 24 TABLET, FILM COATED in 1 BOTTLE
58602-738-12586020738121 BOTTLE in 1 CARTON (58602-738-12) / 40 TABLET, FILM COATED in 1 BOTTLE
58602-738-14586020738141 BOTTLE in 1 CARTON (58602-738-14) / 50 TABLET, FILM COATED in 1 BOTTLE
58602-738-19586020738191 BOTTLE in 1 CARTON (58602-738-19) / 90 TABLET, FILM COATED in 1 BOTTLE
58602-738-21586020738211 BOTTLE in 1 CARTON (58602-738-21) / 100 TABLET, FILM COATED in 1 BOTTLE
58602-738-25586020738251 BOTTLE in 1 CARTON (58602-738-25) / 130 TABLET, FILM COATED in 1 BOTTLE
58602-738-29586020738291 BOTTLE in 1 CARTON (58602-738-29) / 150 TABLET, FILM COATED in 1 BOTTLE
58602-738-34586020738341 BOTTLE in 1 CARTON (58602-738-34) / 200 TABLET, FILM COATED in 1 BOTTLE
58602-738-3858602073838300 TABLET, FILM COATED in 1 BOTTLE (58602-738-38)
58602-738-4058602073840500 TABLET, FILM COATED in 1 BOTTLE (58602-738-40)
58602-738-4458602073844400 TABLET, FILM COATED in 1 BOTTLE (58602-738-44)

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 58602-738 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/58602-738 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 58602-738. 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.