NDC codes

FDA NDC Directory
Product NDC (as listed)50844-417Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50844-0417Add 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
50844-417-11508440417115084404171160 POUCH in 1 CARTON (50844-417-11) / 1 TABLET, FILM COATED in 1 POUCH (50844-417-43)Marketed from Feb 1, 2017
50844-417-145084404171450844041714500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-417-14)Marketed from Feb 1, 2017
50844-417-1650844041716508440417161000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-417-16)Marketed from Feb 1, 2017
50844-417-1950844041719508440417191 BOTTLE, PLASTIC in 1 CARTON (50844-417-19) / 8 TABLET, FILM COATED in 1 BOTTLE, PLASTICMarketed from Feb 1, 2017
50844-417-22508440417225084404172248 POUCH in 1 CARTON (50844-417-22) / 1 TABLET, FILM COATED in 1 POUCH (50844-417-43)Marketed from Feb 1, 2017
50844-417-56508440417565084404175625 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-417-56)Marketed from Feb 1, 2017
50844-417-9850844041798508440417988 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-417-98)Marketed from Feb 1, 2017
50844-417-9950844041799508440417998 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-417-99)Marketed from Feb 1, 2017

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
L.N.K. International, Inc.NDC labeler code 50844
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 204872
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers
Product ID 50844-417_89d3ed35-e75c-41d8-aa99-57cc1fd866d2SPL ID 89d3ed35-e75c-41d8-aa99-57cc1fd866d2SPL set ID 717518e4-2537-4229-b765-c6acfe963d4bRxCUI 849574UNII 9TN87S3A3CUPC 0050844604063, 0050844417168

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

N450844041711 followed by a unit qualifier and the quantity

Package 50844-0417-11. 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: headache muscular aches minor pain of arthritis toothache the common cold menstrual cramps backache temporarily reduces fever

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 50844-417

What is NDC 50844-417?
50844-417 is the product NDC for Naproxen Sodium, Naproxen sodium 220 mg/1 tablet, film coated, listed with the FDA by L.N.K. International, Inc.. It has 8 package NDCs, 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?
L.N.K. International, Inc., NDC labeler code 50844. 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 204872

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

FDA NDC Directory listings under ANDA 204872
ProductStrengthForm · routeLabelerProduct NDC
24/7 Life by 7-Eleven Naproxen Sodiumnaproxen sodium tablet, film coatedNaproxen sodium 220 mg/1Tablet, Film coatedOralLil' Drug Store Products, Inc.66715-5428
All Day Pain Reliefnaproxen sodiumNaproxen sodium 220 mg/1Tablet, Film coatedOralWALMART INC.79903-005
AnaDentnaproxen sodiumNaproxen sodium 220 mg/1Tablet, Film coatedOralBelmora LLC27854-170
Artridolnaproxen sodiumNaproxen sodium 220 mg/1Tablet, Film coatedOralZapotol Products Corp59428-604
Back and Muscle Painnaproxen sodiumNaproxen sodium 220 mg/1Tablet, Film coatedOralRite Aid Corporation11822-4170
Back and Muscle Painnaproxen sodiumNaproxen sodium 220 mg/1Tablet, Film coatedOralCVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED51316-817
First Aid Direct All Day Pain Reliefnaproxen sodiumNaproxen sodium 220 mg/1Tablet, CoatedOralCintas Corporation42961-122
Flanaxnaproxen sodiumNaproxen sodium 220 mg/1Tablet, Film coatedOralBelmora LLC27854-160
Flanax Menstrual Pain Relievernaproxen sodiumNaproxen sodium 220 mg/1Tablet, Film coatedOralBelmora LLC27854-165
Naproxennaproxen sodiumNaproxen sodium 220 mg/1Tablet, Film coatedOralBetter Living Brands, LLC21130-674
Naproxennaproxen sodiumNaproxen sodium 220 mg/1Tablet, Film coatedOralAmerisource Bergen46122-562
Naproxennaproxen sodiumNaproxen sodium 220 mg/1Tablet, Film coatedOralAmerisource Bergen46122-564
Naproxennaproxen sodiumNaproxen sodium 220 mg/1Tablet, Film coatedOralL.N.K. International, Inc.50844-261
Naproxennaproxen sodiumNaproxen sodium 220 mg/1Tablet, Film coatedOralFamily Dollar Services Inc55319-406
Naproxennaproxen sodiumNaproxen sodium 220 mg/1Tablet, Film coatedOralFamily Dollar Services Inc55319-717
Naproxennaproxen sodiumNaproxen sodium 220 mg/1TabletOralGeri-Care Pharmaceutical Corp57896-954
Naproxennaproxen sodiumNaproxen sodium 220 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-5039
Naproxennaproxen sodiumNaproxen sodium 220 mg/1TabletOralPreferred Pharmaceuticals, Inc.68788-7572
Naproxennaproxen sodiumNaproxen sodium 220 mg/1TabletOralProficient Rx LP71205-595
Naproxennaproxen sodiumNaproxen sodium 220 mg/1TabletOralBryant Ranch Prepack71335-1282

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