NDC codes

FDA NDC Directory
Product NDC (as listed)30142-954Labeler and product segments. Claims need a package NDC.
Product NDC at billing width30142-0954Add 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
30142-954-10301420954101 BOTTLE in 1 CARTON (30142-954-10) / 100 TABLET, COATED in 1 BOTTLEMarketed from Aug 4, 2021
30142-954-20301420954201 BOTTLE in 1 CARTON (30142-954-20) / 200 TABLET, COATED in 1 BOTTLEMarketed from Aug 4, 2021
30142-954-50301420954501 BOTTLE in 1 CARTON (30142-954-50) / 500 TABLET, COATED in 1 BOTTLEMarketed from Aug 4, 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, Coated
Route
Oral
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 075168
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers
Product ID 30142-954_ee849c66-1cf3-2a24-16bf-8b8c36198f07SPL ID ee849c66-1cf3-2a24-16bf-8b8c36198f07SPL set ID 30bcf289-0039-f389-73c4-fef3e8861034RxCUI 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

N430142095410 followed by a unit qualifier and the quantity

Package 30142-0954-10. 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 ANDA 075168

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

FDA NDC Directory listings under ANDA 075168
ProductStrengthForm · routeLabelerProduct NDC
Naproxen SodiumNaproxen sodium 220 mg/1Tablet, CoatedOralSAM'S WEST INC68196-255
Naproxen SodiumNaproxen sodium 220 mg/1Tablet, CoatedOralDr.Reddy's Laboratories Limited55111-273
Naproxen SodiumNaproxen sodium 220 mg/1Tablet, CoatedOralDr.Reddy's Laboratories Limited55111-272
Naproxen Sodium Headache Pain Capletsnaproxen sodiumNaproxen sodium 220 mg/1Tablet, CoatedOralDr.Reddy's Laboratories Inc43598-059
Naproxen Sodium Capletsnaproxen sodiumNaproxen sodium 220 mg/1Tablet, CoatedOralDr Reddy's Laboratories Inc43598-058
Naproxen Sodium Back and Muscle Pain Capletsnaproxen sodiumNaproxen sodium 220 mg/1Tablet, CoatedOralDr.Reddy's Laboratories Inc43598-060
Naproxen Sodium Back and Muscle Painnaproxen sodiumNaproxen sodium 220 mg/1Tablet, CoatedOralDr.Reddy's Laboratories Inc43598-073
Naproxen Sodium Headache Painnaproxen sodiumNaproxen sodium 220 mg/1Tablet, CoatedOralDr.Reddy's Laboratories Inc43598-071
Naproxen Sodium Headache Painnaproxen sodiumNaproxen sodium 220 mg/1Tablet, CoatedOralDr.Reddy's Laboratories Inc43598-072
Naproxen Sodium Back and Muscle Painnaproxen sodiumNaproxen sodium 220 mg/1Tablet, CoatedOralDr.Reddy's Laboratories Inc43598-074

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