NDC codes

FDA NDC Directory
Product NDC (as listed)43598-494Labeler and product segments. Claims need a package NDC.
Product NDC at billing width43598-0494Add 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
43598-494-014359804940143598049401100 TABLET, FILM COATED in 1 BOTTLE (43598-494-01)Marketed from Apr 26, 2016
43598-494-054359804940543598049405500 TABLET, FILM COATED in 1 BOTTLE (43598-494-05)Marketed from Apr 26, 2016
43598-494-1043598049410435980494101000 TABLET, FILM COATED in 1 BOTTLE (43598-494-10)Marketed from Apr 26, 2016
43598-494-30435980494304359804943030 TABLET, FILM COATED in 1 BOTTLE (43598-494-30)Marketed from Apr 26, 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)
Naproxen sodium
Generic name (nonproprietary)
naproxen sodium
Active ingredients
Naproxen sodium — 275 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
Dr. Reddy's Laboratories Inc.NDC labeler code 43598
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 078486
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers
Product ID 43598-494_b0e85222-c6c4-647a-6fd1-e38676517e2aSPL ID b0e85222-c6c4-647a-6fd1-e38676517e2a

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

N443598049401 followed by a unit qualifier and the quantity

Package 43598-0494-01. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 43598-494

What is NDC 43598-494?
43598-494 is the product NDC for Naproxen sodium, Naproxen sodium 275 mg/1 tablet, film coated, listed with the FDA by Dr. Reddy's Laboratories Inc.. It has 4 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?
Dr. Reddy's Laboratories Inc., NDC labeler code 43598. 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 078486

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

FDA NDC Directory listings under ANDA 078486
ProductStrengthForm · routeLabelerProduct NDC
Naproxen sodiumNaproxen sodium 550 mg/1Tablet, Film coatedOralDr. Reddy's Laboratories Inc.43598-495
Naproxen sodiumNaproxen sodium 550 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-5238
Naproxen sodiumNaproxen sodium 550 mg/1Tablet, Film coatedOralQuality Care Products, LLC55700-625
Naproxen sodiumNaproxen sodium 550 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-1650
Naproxen sodiumNaproxen sodium 550 mg/1Tablet, Film coatedOralPHOENIX RX LLC85509-1495

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