What is NDC 71335-0255?

71335-0255 is the product NDC for Naproxen, Naproxen 375 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 8 package NDCs, shown above in 10- and 11-digit form.

Bryant Ranch Prepack, NDC labeler code 71335. 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?

185 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Naproxen NDC 71335-0255 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)71335-0255Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71335-0255Add 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 NDC	11-digit (billing)	Package
71335-0255-1	71335025501	20 TABLET in 1 BOTTLE (71335-0255-1)Marketed from Oct 2, 2017
71335-0255-2	71335025502	30 TABLET in 1 BOTTLE (71335-0255-2)Marketed from Oct 2, 2017
71335-0255-3	71335025503	40 TABLET in 1 BOTTLE (71335-0255-3)Marketed from Oct 2, 2017
71335-0255-4	71335025504	120 TABLET in 1 BOTTLE (71335-0255-4)Marketed from Oct 2, 2017
71335-0255-5	71335025505	60 TABLET in 1 BOTTLE (71335-0255-5)Marketed from Oct 2, 2017
71335-0255-6	71335025506	90 TABLET in 1 BOTTLE (71335-0255-6)Marketed from Oct 2, 2017
71335-0255-7	71335025507	14 TABLET in 1 BOTTLE (71335-0255-7)Marketed from Oct 2, 2017
71335-0255-8	71335025508	15 TABLET in 1 BOTTLE (71335-0255-8)Marketed from Oct 2, 2017

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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
Generic name (nonproprietary): naproxen
Active ingredients: Naproxen — 375 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Bryant Ranch PrepackNDC labeler code 71335
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 091416
Marketing start: Jul 6, 2016
Listing expires: Dec 31, 2026
Other FDA classes: Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers: Product ID 71335-0255_f6ea33a2-ec65-4b5d-9fb8-d8beb4cc2138SPL ID f6ea33a2-ec65-4b5d-9fb8-d8beb4cc2138SPL set ID 5d399bf3-db49-411a-91b9-b410d702a65aRxCUI 198012, 198013UNII 57Y76R9ATQ
Pharmacologic class: Nonsteroidal Anti-inflammatory Drug

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

N471335025501 followed by a unit qualifier and the quantity

Package 71335-0255-01. 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

Current FDA label (SPL), effective Dec 14, 2020.

Indications (excerpt from the label)

CAREFULLY CONSIDER THE POTENTIAL BENEFITS AND RISKS OF NAPROXEN AND OTHER TREATMENT OPTIONS BEFORE DECIDING TO USE NAPROXEN TABLETS. USE THE LOWEST EFFECTIVE DOSE FOR THE SHORTEST DURATION CONSISTENT WITH INDIVIDUAL PATIENT TREATMENT GOALS (SEE WARNINGS: GASTROINTESTINAL BLEEDING, ULCERATION, AND PERFORATION). NAPROXEN TABLETS ARE INDICATED: FOR THE RELIEF OF THE SIGNS AND SYMPTOMS OF RHEUMATOID ARTHRITIS. FOR THE RELIEF OF THE SIGNS AND SYMPTOMS OF OSTEOARTHRITIS FOR THE RELIEF OF THE SIGNS AND SYMPTOMS OF ANKYLOSING SPONDYLITIS FOR THE RELIEF OF THE SIGNS AND SYMPTOMS OF JUVENILE ARTHRITIS NAPROXEN TABLETS ARE ALSO INDICATED: FOR RELIEF OF THE SIGNS AND SYMPTOMS OF TENDONITIS FOR RELIEF OF…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71335-0255

What is NDC 71335-0255?: 71335-0255 is the product NDC for Naproxen, Naproxen 375 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 8 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Naproxen.
What is the active ingredient?: Naproxen.
Who is the labeler?: Bryant Ranch Prepack, NDC labeler code 71335. 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?: 185 other product NDCs are listed under this name. See all Naproxen 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 NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Naproxen	Naproxen 500 mg/1	TabletOral	REMEDYREPACK INC.	70518-4750	70518-4750-00
Naproxen	Naproxen 500 mg/1	TabletOral	Coupler LLC	67046-0784	67046-0784-03
Naproxen	Naproxen 250 mg/1	TabletOral	Coupler LLC	67046-0499	67046-0499-03
Naproxen	Naproxen 375 mg/1	TabletOral	Coupler LLC	67046-0500	67046-0500-03
Naproxen	Naproxen 500 mg/1	TabletOral	Coupler LLC	67046-0501	67046-0501-03
Naproxen	Naproxen 375 mg/1	Tablet, Delayed releaseOral	Sunrise Pharmaceutical, Inc.	11534-211	11534-0211-01
Naproxen	Naproxen 500 mg/1	Tablet, Delayed releaseOral	Sunrise Pharmaceutical, Inc.	11534-212	11534-0212-01
Naproxen	Naproxen 250 mg/1	TabletOral	REMEDYREPACK INC.	70518-4514	70518-4514-00
Naproxen	Naproxen 500 mg/1	TabletOral	Medcore LLC	82461-711	82461-0711-60
Naproxen	Naproxen 125 mg/5mL	SuspensionOral	Aurobindo Pharma Limited	59651-528	59651-0528-47

All 186 Naproxen NDCs

Other NDCs under ANDA 091416

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

FDA NDC Directory listings under ANDA 091416
Product	Strength	Form · route	Labeler	Product NDC
Naproxen	Naproxen 500 mg/1	TabletOral	Northwind Health Company, LLC	51655-621
Naproxen	Naproxen 375 mg/1	TabletOral	MARKSANS PHARMA LIMITED	25000-139
Naproxen	Naproxen 500 mg/1	TabletOral	MARKSANS PHARMA LIMITED	25000-140
Naproxen	Naproxen 500 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-4006
Naproxen	Naproxen 500 mg/1	TabletOral	Aphena Pharma Solutions - Tennessee, LLC	71610-436
Naproxen	Naproxen 500 mg/1	TabletOral	TIME CAP LABORATORIES	49483-618
Naproxen	Naproxen 375 mg/1	TabletOral	TIME CAP LABORATORIES	49483-617
Naproxen	Naproxen 250 mg/1	TabletOral	MARKSANS PHARMA LIMITED	25000-138
Naproxen	Naproxen 250 mg/1	TabletOral	TIME CAP LABORATORIES	49483-619
Naproxen	Naproxen 500 mg/1	TabletOral	QPharma Inc	42708-140
Naproxen	Naproxen 500 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-4381
Naproxen	Naproxen 250 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-4510
Naproxen	Naproxen 250 mg/1	TabletOral	Bryant Ranch Prepack	71335-0973
Naproxen	Naproxen 500 mg/1	TabletOral	Asclemed USA, Inc.	76420-042
Naproxen	Naproxen 500 mg/1	TabletOral	DIRECT RX	72189-136
Naproxen	Naproxen 375 mg/1	TabletOral	Advanced Rx of Tennessee, LLC	80425-0048
Naproxen	Naproxen 500 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	43063-920