NDC codes

FDA NDC Directory
Product NDC (as listed)69517-109Labeler and product segments. Claims need a package NDC.
Product NDC at billing width69517-0109Add 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
69517-109-0269517010902695170109022 POUCH in 1 POUCH (69517-109-02) / 2 TABLET in 1 POUCHMarketed from Apr 7, 2016
69517-109-046951701090469517010904400 BOTTLE in 1 BOTTLE (69517-109-04) / 100 BOTTLE in 1 BOTTLE (69517-109-01) / 24 CARTON in 1 BOTTLE (69517-109-24) / 1 TABLET in 1 CARTONMarketed from Apr 7, 2016
69517-109-25695170109256951701092525 POUCH in 1 BOX (69517-109-25) / 2 TABLET in 1 POUCHMarketed from Apr 7, 2016
69517-109-50695170109506951701095050 POUCH in 1 BOX (69517-109-50) / 2 TABLET in 1 POUCHMarketed from Apr 7, 2016

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)
All Day Pain Relief
Generic name (nonproprietary)
naproxen sodium tablets, 220 mg
Active ingredients
Naproxen sodium — 220 mg/1
Dosage form
Tablet
Route
Oral
Labeler
HealthLife of USA LLCNDC labeler code 69517
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 091353
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers
Product ID 69517-109_046b91ed-d78b-42c0-b822-77fcbdeff84bSPL ID 046b91ed-d78b-42c0-b822-77fcbdeff84bSPL set ID 7b0cb91e-5465-40ef-9f82-919f7d984f17RxCUI 849574UNII 9TN87S3A3CUPC 0069517109248

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

N469517010902 followed by a unit qualifier and the quantity

Package 69517-0109-02. 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 ■ backache ■ headache ■ menstrual cramps ■ 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 69517-109

What is NDC 69517-109?
69517-109 is the product NDC for All Day Pain Relief, Naproxen sodium 220 mg/1 tablet, listed with the FDA by HealthLife of USA LLC. It has 4 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
All Day Pain Relief (Naproxen Sodium Tablets, 220 mg).
What is the active ingredient?
Naproxen sodium.
Who is the labeler?
HealthLife of USA LLC, NDC labeler code 69517. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for All Day Pain Relief?
9 other product NDCs are listed under this name. See all All Day Pain Relief 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 All Day Pain Relief NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
All Day Pain Reliefnaproxen sodiumNaproxen sodium 220 mg/1TabletOralWalmart Inc.79903-38979903-0389-50
All Day Pain Reliefnaproxen sodiumNaproxen sodium 220 mg/1Tablet, Film coatedOralWALMART INC.79903-00579903-0005-2079903-0005-2579903-0005-27+1 more
All Day Pain Reliefnaproxen sodiumNaproxen sodium 220 mg/1Tablet, CoatedOralWALGREENS0363-609900363-6099-0100363-6099-0500363-6099-20
All Day Pain Reliefnaproxen sodiumNaproxen sodium 220 mg/1Tablet, CoatedOralWALGREENS0363-960800363-9608-0500363-9608-0900363-9608-20+4 more
All Day Pain Reliefnaproxen sodiumNaproxen sodium 220 mg/1TabletOralH E B37808-06837808-0068-2437808-0068-50
all day pain reliefnaproxen sodiumNaproxen sodium 200 mg/1Tablet, Film coatedOralWalgreen Company0363-093800363-0938-82
All Day Pain Reliefnaproxen sodiumNaproxen sodium 220 mg/1Tablet, CoatedOralVALU MERCHANDISERS COMPANY63941-14463941-0144-0163941-0144-0263941-0144-03
All Day Pain Reliefnaproxen sodiumNaproxen sodium 220 mg/1Tablet, CoatedOralVALU MERCHANDISERS COMPANY63941-24563941-0245-0163941-0245-0263941-0245-03
All Day Pain Reliefnaproxen sodiumNaproxen sodium 220 mg/1Tablet, Film coatedOralWalgreen Company0363-036800363-0368-7100363-0368-7500363-0368-76

Other NDCs under ANDA 091353

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

FDA NDC Directory listings under ANDA 091353
ProductStrengthForm · routeLabelerProduct NDC
Dr Simi All Day Pain Reliefnaproxen sodiumNaproxen sodium 220 mg/1Tablet, Film coatedOralFarmacias De Similares TX LLC85786-104
NaproxenNaproxen sodium 220 mg/1TabletOralSafeway, Inc21130-062
Naproxen SodiumNaproxen sodium 220 mg/1TabletOralTARGET CORPORATION11673-764
Naproxen SodiumNaproxen sodium 220 mg/1TabletOralSafeway, Inc21130-061
Naproxen SodiumNaproxen sodium 220 mg/1TabletOralCVS51316-761
Naproxen SodiumNaproxen sodium 220 mg/1TabletOralCVS51316-762
Naproxen SodiumNaproxen sodium 220 mg/1TabletOralGranules India Ltd62207-327
Naproxen SodiumNaproxen sodium 220 mg/1TabletOralGranules India Ltd62207-328
Naproxen SodiumNaproxen sodium 220 mg/1TabletOralGranules India Ltd62207-728
Naproxen SodiumNaproxen sodium 220 mg/1TabletOralGranules India Ltd62207-729
Naproxen SodiumNaproxen sodium 220 mg/1Tablet, Film coatedOralGranules India Ltd62207-761
Naproxen SodiumNaproxen sodium 220 mg/1Tablet, Film coatedOralGranules India Ltd62207-762
Naproxen SodiumNaproxen sodium 220 mg/1Tablet, Film coated, Extended releaseOralSPIRIT PHARMACEUTICALS,LLC68210-4096
Naproxen SodiumNaproxen sodium 220 mg/1TabletOralGranules USA, Inc.69848-010
Pain Reliefnaproxen sodiumNaproxen sodium 220 mg/1Tablet, Film coatedOralGobrands, Inc82501-1576
Proxen Np 660naproxen sodiumNaproxen sodium 220 mg/1TabletOralOPMX LLC69729-123
Rapidol Naproxennaproxen sodiumNaproxen sodium 220 mg/1Tablet, CoatedOralPharmadel LLC55758-048

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