Prescription drug · NDA AUTHORIZED GENERIC

Naproxen Sodium NDC 24979-254

Naproxen sodium 750 mg/1 · Tablet, Film coated, Extended release · Oral · Upsher-Smith Laboratories, LLC

NDC codes

FDA NDC Directory
Product NDC (as listed)24979-254Labeler and product segments. Claims need a package NDC.
Product NDC at billing width24979-0254Add 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
24979-254-062497902540630 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (24979-254-06)Marketed from Apr 25, 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 — 750 mg/1
Dosage form
Tablet, Film coated, Extended release
Route
Oral
Product type
Prescription drug
Marketing category
NDA authorized genericApplication NDA 020353
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers
Product ID 24979-254_a79a3bf0-fe2f-4ba4-8eaa-e1c97ab9b927SPL ID a79a3bf0-fe2f-4ba4-8eaa-e1c97ab9b927SPL set ID 7c22a2d6-821c-4f83-aead-e756aed930e5RxCUI 1116320, 1116339, 1116349UNII 9TN87S3A3CUPC 0324979252018, 0324979254067, 0324979253688

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

N424979025406 followed by a unit qualifier and the quantity

Package 24979-0254-06. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

Naproxen Sodium Controlled-Release Tablets are indicated for the treatment of: rheumatoid arthritis (RA) osteoarthritis (OA) ankylosing spondylitis (AS) tendinitis, bursitis acute gout primary dysmenorrhea (PD) the relief of mild to moderate pain [ see Warnings and Precautions ( 5 ) ]. Naproxen Sodium Controlled-Release Tablets is a nonsteroidal anti-inflammatory drug indicated for the treatment of: rheumatoid arthritis (RA)( 1 ) osteoarthritis (OA)( 1 ) ankylosing spondylitis (AS)( 1 ) tendinitis, bursitis ( 1 ) acute gout ( 1 ) primary dysmenorrhea (PD)( 1 ) the relief of mild to moderate pain ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

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 500 mg/1Tablet, Film coated, Extended releaseOralAlvogen Inc.47781-154
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
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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Naproxen Sodium NDC 24979-254 | Med-Code