NDC codes

FDA NDC Directory
Product NDC (as listed)79903-232Labeler and product segments. Claims need a package NDC.
Product NDC at billing width79903-0232Add 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
79903-232-9079903023290799030232901 BOTTLE in 1 CARTON (79903-232-90) / 90 TABLET, FILM COATED in 1 BOTTLEMarketed from Feb 14, 2024

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
Generic name (nonproprietary)
naproxen sodium
Active ingredients
Naproxen sodium — 220 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
WALMART INC.NDC labeler code 79903
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 79903-232_9641a476-de98-47f1-b608-d687aaba9e42SPL ID 9641a476-de98-47f1-b608-d687aaba9e42SPL set ID 1292c0ca-343e-adcc-e063-6394a90ab9faRxCUI 849574UNII 9TN87S3A3CUPC 0194346189090

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

N479903023290 followed by a unit qualifier and the quantity

Package 79903-0232-90. 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: minor pain of arthritis muscular aches menstrual cramps toothache backache headache 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 79903-232

What is NDC 79903-232?
79903-232 is the product NDC for Naproxen Sodium, Naproxen sodium 220 mg/1 tablet, film coated, listed with the FDA by WALMART INC.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Naproxen Sodium.
What is the active ingredient?
Naproxen sodium.
Who is the labeler?
WALMART INC., NDC labeler code 79903. 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?
144 other product NDCs are listed under this name. See all Naproxen Sodium 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 NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
naproxen sodiumNaproxen sodium 220 mg/1Tablet, Film coatedOralAmazon.com Services LLC72288-98872288-0988-75
Naproxen SodiumNaproxen sodium 220 mg/1Tablet, CoatedOralAAA Pharmaceutical, Inc.57344-24457344-0244-03
Naproxen SodiumNaproxen sodium 550 mg/1TabletOralAdvanced Rx of Tennessee, LLC80425-057480425-0574-0180425-0574-0280425-0574-03
Naproxen SodiumNaproxen sodium 220 mg/1Tablet, CoatedOralHYVEE INC42507-24542507-0245-0142507-0245-0842507-0245-14
Naproxen SodiumNaproxen sodium 220 mg/1Tablet, CoatedOralHYVEE INC42507-84442507-0844-0142507-0844-14
Naproxen SodiumNaproxen sodium 220 mg/1Capsule, Liquid filledOralTARGET Corporation11673-65111673-0651-78
Naproxen SodiumNaproxen sodium 220 mg/1Tablet, Film coatedOralSafeway21130-59321130-0593-79
Naproxen SodiumNaproxen sodium 550 mg/1TabletOralAdvanced Rx of Tennessee, LLC80425-053180425-0531-0180425-0531-0280425-0531-03
Naproxen SodiumNaproxen sodium 550 mg/1TabletOralAdvanced Rx of Tennessee, LLC80425-053280425-0532-0180425-0532-0280425-0532-03
Naproxen SodiumNaproxen sodium 220 mg/1Tablet, CoatedOralCHAIN DRUG MARKETING ASSOCIATION, INC.83324-10883324-0108-0183324-0108-2483324-0108-50

All 145 Naproxen Sodium NDCs

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.79903-231
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
Naproxen Sodium BACK AND MUSCLE PAINnaproxen sodiumNaproxen sodium 220 mg/1Tablet, Film coatedOralAurohealth LLC58602-739
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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