NDC codes

FDA NDC Directory
Product NDC (as listed)58602-739Labeler and product segments. Claims need a package NDC.
Product NDC at billing width58602-0739Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
58602-739-0758602073907586020739071 BOTTLE in 1 CARTON (58602-739-07) / 24 TABLET, FILM COATED in 1 BOTTLEMarketed from Jul 14, 2021
58602-739-1258602073912586020739121 BOTTLE in 1 CARTON (58602-739-12) / 40 TABLET, FILM COATED in 1 BOTTLEMarketed from Jul 14, 2021
58602-739-1958602073919586020739191 BOTTLE in 1 CARTON (58602-739-19) / 90 TABLET, FILM COATED in 1 BOTTLEMarketed from Aug 2, 2024
58602-739-2158602073921586020739211 BOTTLE in 1 CARTON (58602-739-21) / 100 TABLET, FILM COATED in 1 BOTTLEMarketed from Jul 14, 2021
58602-739-2558602073925586020739251 BOTTLE in 1 CARTON (58602-739-25) / 130 TABLET, FILM COATED in 1 BOTTLEMarketed from Jul 14, 2021
58602-739-2958602073929586020739291 BOTTLE in 1 CARTON (58602-739-29) / 150 TABLET, FILM COATED in 1 BOTTLEMarketed from Jul 14, 2021
58602-739-3458602073934586020739341 BOTTLE in 1 CARTON (58602-739-34) / 200 TABLET, FILM COATED in 1 BOTTLEMarketed from Jul 14, 2021
58602-739-3858602073938586020739381 BOTTLE in 1 CARTON (58602-739-38) / 300 TABLET, FILM COATED in 1 BOTTLEMarketed from Jul 14, 2021
58602-739-4058602073940586020739401 BOTTLE in 1 CARTON (58602-739-40) / 500 TABLET, FILM COATED in 1 BOTTLEMarketed from Jul 14, 2021
58602-739-445860207394458602073944400 TABLET, FILM COATED in 1 BOTTLE (58602-739-44)Marketed from Jul 14, 2021
58602-739-7858602073978586020739781 BOTTLE in 1 CARTON (58602-739-78) / 50 TABLET, FILM COATED in 1 BOTTLEMarketed from Jul 14, 2021

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary)
Naproxen Sodium BACK AND MUSCLE PAIN
Generic name (nonproprietary)
naproxen sodium
Active ingredients
Naproxen sodium — 220 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
Aurohealth LLCNDC labeler code 58602
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 205497
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers
Product ID 58602-739_ff1010cd-0fc3-4e54-8a03-f3dfa1417926SPL ID ff1010cd-0fc3-4e54-8a03-f3dfa1417926SPL set ID 666e3c6a-e571-4124-84d8-0142db1012dcRxCUI 849574UNII 9TN87S3A3C

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N458602073907 followed by a unit qualifier and the quantity

Package 58602-0739-07. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective .

Indications (excerpt from the label)

Uses temporarily relieves minor aches and pains due to: backache muscular aches minor pain of arthritis menstrual cramps headache toothache the common cold temporarily reduces fever

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 58602-739

What is NDC 58602-739?
58602-739 is the product NDC for Naproxen Sodium BACK AND MUSCLE PAIN, Naproxen sodium 220 mg/1 tablet, film coated, listed with the FDA by Aurohealth LLC. It has 11 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Naproxen Sodium BACK AND MUSCLE PAIN (Naproxen Sodium).
What is the active ingredient?
Naproxen sodium.
Who is the labeler?
Aurohealth LLC, NDC labeler code 58602. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Naproxen Sodium BACK AND MUSCLE PAIN?
3 other product NDCs are listed under this name. See all Naproxen Sodium BACK AND MUSCLE PAIN NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Naproxen Sodium BACK AND MUSCLE PAIN NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Naproxen Sodium Back and Muscle Painnaproxen sodiumNaproxen sodium 220 mg/1Tablet, CoatedOralDr.Reddy's Laboratories Inc43598-07343598-0073-01
Naproxen Sodium Back and Muscle Painnaproxen sodiumNaproxen sodium 220 mg/1Tablet, CoatedOralDr.Reddy's Laboratories Inc43598-07443598-0074-01
Naproxen Sodium BACK AND MUSCLE PAINnaproxen sodiumNaproxen sodium 220 mg/1Tablet, Film coatedOralAurohealth LLC58602-73658602-0736-0758602-0736-1958602-0736-21+4 more

Other NDCs under ANDA 205497

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 205497
ProductStrengthForm · routeLabelerProduct NDC
Naproxen SodiumNaproxen sodium 220 mg/1Tablet, Film coatedOralWALMART INC.79903-232
Naproxen SodiumNaproxen sodium 220 mg/1Tablet, Film coatedOralWALMART INC.79903-231
Amazon Basic Care Naproxen Sodiumnaproxen sodiumNaproxen sodium 220 mg/1Tablet, Film coatedOralAmazon.com Services LLC72288-366
Naproxen Sodium HEADACHE PAINnaproxen sodiumNaproxen sodium 220 mg/1Tablet, Film coatedOralAurohealth LLC58602-737
Naproxen Sodium HEADACHE PAINnaproxen sodiumNaproxen sodium 220 mg/1Tablet, Film coatedOralAurohealth LLC58602-735
Naproxen Sodium BACK AND MUSCLE PAINnaproxen sodiumNaproxen sodium 220 mg/1Tablet, Film coatedOralAurohealth LLC58602-736
Naproxen SodiumNaproxen sodium 220 mg/1Tablet, Film coatedOralAurohealth LLC58602-738
Flanax Pain Reliever/Fever Reducernaproxen sodiumNaproxen sodium 220 mg/1Tablet, Film coatedOralBelmora LLC27854-700
Ana-Dent PAIN RELIEFnaproxen sodiumNaproxen sodium 220 mg/1Tablet, Film coatedOralBelmora LLC27854-701
Naproxen SodiumNaproxen sodium 220 mg/1Tablet, Film coatedOralAurohealth LLC58602-819
Naproxen SodiumNaproxen sodium 220 mg/1Tablet, Film coatedOralAurohealth LLC58602-845

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