NDC codes

FDA NDC Directory
Product NDC (as listed)62207-327Labeler and product segments. Claims need a package NDC.
Product NDC at billing width62207-0327Add 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
62207-327-41622070327416220703274124 TABLET in 1 BOTTLE (62207-327-41)Marketed from Jul 16, 2021
62207-327-42622070327426220703274250 TABLET in 1 BOTTLE (62207-327-42)Marketed from Jul 16, 2021
62207-327-436220703274362207032743100 TABLET in 1 BOTTLE (62207-327-43)Marketed from Jul 16, 2021
62207-327-476220703274762207032747500 TABLET in 1 BOTTLE (62207-327-47)Marketed from Jul 16, 2021
62207-327-4962207032749622070327491000 TABLET in 1 BOTTLE (62207-327-49)Marketed from Jul 16, 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
Generic name (nonproprietary)
naproxen sodium
Active ingredients
Naproxen sodium — 220 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Granules India LtdNDC labeler code 62207
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 62207-327_f4026a0a-c9cd-3850-e053-2995a90a459cSPL ID f4026a0a-c9cd-3850-e053-2995a90a459cSPL set ID 95ba1722-60ed-4a83-9f26-50c4de8cf180RxCUI 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

N462207032741 followed by a unit qualifier and the quantity

Package 62207-0327-41. 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)

USE(S) • temporarily relieves minor aches and pains due to: • minor pain of arthritis • muscular aches • backache • 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 62207-327

What is NDC 62207-327?
62207-327 is the product NDC for Naproxen Sodium, Naproxen sodium 220 mg/1 tablet, listed with the FDA by Granules India Ltd. It has 5 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?
Granules India Ltd, NDC labeler code 62207. 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 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
Pain Reliefnaproxen sodiumNaproxen sodium 220 mg/1Tablet, Film coatedOralGobrands, Inc82501-1576
All Day Pain Reliefnaproxen sodium tablets, 220 mgNaproxen sodium 220 mg/1TabletOralHealthLife of USA LLC69517-109
Dr Simi All Day Pain Reliefnaproxen sodiumNaproxen sodium 220 mg/1Tablet, Film coatedOralFarmacias De Similares TX LLC85786-104
Naproxen SodiumNaproxen sodium 220 mg/1TabletOralTARGET CORPORATION11673-764
Naproxen SodiumNaproxen sodium 220 mg/1TabletOralSafeway, Inc21130-061
NaproxenNaproxen sodium 220 mg/1TabletOralSafeway, Inc21130-062
Naproxen SodiumNaproxen sodium 220 mg/1TabletOralBi-Mart37835-594
Naproxen SodiumNaproxen sodium 220 mg/1TabletOralGranules India Ltd62207-328
Naproxen SodiumNaproxen sodium 220 mg/1TabletOralCVS51316-761
Naproxen SodiumNaproxen sodium 220 mg/1TabletOralCVS51316-762
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 coated, Extended releaseOralSPIRIT PHARMACEUTICALS,LLC68210-4096
Rapidol Naproxennaproxen sodiumNaproxen sodium 220 mg/1Tablet, CoatedOralPharmadel LLC55758-048
Naproxen SodiumNaproxen sodium 220 mg/1Tablet, Film coatedOralGranules India Ltd62207-761
Naproxen SodiumNaproxen sodium 220 mg/1Tablet, Film coatedOralGranules India Ltd62207-762
Proxen Np 660naproxen sodiumNaproxen sodium 220 mg/1TabletOralOPMX LLC69729-123
Naproxen SodiumNaproxen sodium 220 mg/1TabletOralGranules USA, Inc.69848-010

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