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Naproxen Sodium HEADACHE PAIN

NDC 58602-735, Naproxen Sodium, tablet, film coated, from Aurohealth LLC.

Product NDC
58602-735
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/58602-735 \
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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
58602-735-07586020735071 BOTTLE in 1 CARTON (58602-735-07) / 24 TABLET, FILM COATED in 1 BOTTLE
58602-735-19586020735191 BOTTLE in 1 CARTON (58602-735-19) / 90 TABLET, FILM COATED in 1 BOTTLE
58602-735-21586020735211 BOTTLE in 1 CARTON (58602-735-21) / 100 TABLET, FILM COATED in 1 BOTTLE
58602-735-29586020735291 BOTTLE in 1 CARTON (58602-735-29) / 150 TABLET, FILM COATED in 1 BOTTLE
58602-735-38586020735381 BOTTLE in 1 CARTON (58602-735-38) / 300 TABLET, FILM COATED in 1 BOTTLE
58602-735-40586020735401 BOTTLE in 1 CARTON (58602-735-40) / 500 TABLET, FILM COATED in 1 BOTTLE
58602-735-78586020735781 BOTTLE in 1 CARTON (58602-735-78) / 50 TABLET, FILM 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 58602-735 from code or an agent

curl
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  -H "Authorization: Bearer $HDEV_API_KEY"
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.