NDC codes

FDA NDC Directory
Product NDC (as listed)47781-154Labeler and product segments. Claims need a package NDC.
Product NDC at billing width47781-0154Add 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
47781-154-754778101547575 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47781-154-75)Marketed from Mar 11, 2015

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 — 500 mg/1
Dosage form
Tablet, Film coated, Extended release
Route
Oral
Product type
Prescription drug
Marketing category
NDA authorized genericApplication NDA 020353
Marketing start
Marketing end
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers
Product ID 47781-154_6a207289-a8f0-9db1-548f-b55af6131677SPL ID 6a207289-a8f0-9db1-548f-b55af6131677SPL set ID 9225acaa-209f-958b-2c51-9a46995dec33RxCUI 1116320, 1116339, 1116349UNII 9TN87S3A3CUPC 0347781153014, 0347781155308, 0347781154752

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

N447781015475 followed by a unit qualifier and the quantity

Package 47781-0154-75. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under NDA 020353

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

FDA NDC Directory listings under NDA 020353
ProductStrengthForm · routeLabelerProduct NDC
Naproxen SodiumNaproxen sodium 375 mg/1Tablet, Film coated, Extended releaseOralUpsher-Smith Laboratories, LLC24979-252
Naprelannaproxen sodiumNaproxen sodium 375 mg/1Tablet, Film coated, Extended releaseOralUpsher-Smith Laboratories, LLC24979-249
Naprelannaproxen sodiumNaproxen sodium 500 mg/1Tablet, Film coated, Extended releaseOralUpsher-Smith Laboratories, LLC24979-250
Naprelannaproxen sodiumNaproxen sodium 750 mg/1Tablet, Film coated, Extended releaseOralUpsher-Smith Laboratories, LLC24979-251
Naproxen SodiumNaproxen sodium 500 mg/1Tablet, Film coated, Extended releaseOralUpsher-Smith Laboratories, LLC24979-253
Naproxen SodiumNaproxen sodium 750 mg/1Tablet, Film coated, Extended releaseOralUpsher-Smith Laboratories, LLC24979-254
Naprelannaproxen sodiumNaproxen sodium 375 mg/1Tablet, Film coated, Extended releaseOralAlmatica Pharma LLC52427-272
Naprelannaproxen sodiumNaproxen sodium 500 mg/1Tablet, Film coated, Extended releaseOralAlmatica Pharma LLC52427-273
Naproxen SodiumNaproxen sodium 375 mg/1Tablet, Film coated, Extended releaseOralSA3, LLC69420-1375
Naproxen SodiumNaproxen sodium 375 mg/1Tablet, Film coated, Extended releaseOralAlvogen Inc.47781-153

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