What is NDC 66267-153?

66267-153 is the product NDC for Naproxen, Naproxen 500 mg/1 tablet, listed with the FDA by NuCare Pharmaceuticals, Inc.. It has 9 package NDCs, shown above in 10- and 11-digit form.

NuCare Pharmaceuticals, Inc., NDC labeler code 66267. 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?

189 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 66267-153 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)66267-153Labeler and product segments. Claims need a package NDC.

Product NDC at billing width66267-0153Add 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
66267-153-10	6626701531066267015310	10 TABLET in 1 BOTTLE (66267-153-10)Marketed from Oct 10, 2016
66267-153-14	6626701531466267015314	14 TABLET in 1 BOTTLE (66267-153-14)Marketed from Oct 10, 2016
66267-153-15	6626701531566267015315	15 TABLET in 1 BOTTLE (66267-153-15)Marketed from Oct 10, 2016
66267-153-20	6626701532066267015320	20 TABLET in 1 BOTTLE (66267-153-20)Marketed from Oct 10, 2016
66267-153-30	6626701533066267015330	30 TABLET in 1 BOTTLE (66267-153-30)Marketed from Oct 10, 2016
66267-153-40	6626701534066267015340	40 TABLET in 1 BOTTLE (66267-153-40)Marketed from Oct 10, 2016
66267-153-42	6626701534266267015342	42 TABLET in 1 BOTTLE (66267-153-42)Marketed from Oct 10, 2016
66267-153-60	6626701536066267015360	60 TABLET in 1 BOTTLE (66267-153-60)Marketed from Oct 10, 2016
66267-153-90	6626701539066267015390	90 TABLET in 1 BOTTLE (66267-153-90)Marketed from Oct 10, 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
Generic name (nonproprietary): naproxen
Active ingredients: Naproxen — 500 mg/1
Dosage form: Tablet
Route: Oral
Labeler: NuCare Pharmaceuticals, Inc.NDC labeler code 66267
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 078250
Marketing start: Jul 1, 2007
Listing expires: Dec 31, 2026
Other FDA classes: Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers: Product ID 66267-153_1f98cfb6-fa4d-2288-e063-6294a90a4de7SPL ID 1f98cfb6-fa4d-2288-e063-6294a90a4de7SPL set ID 3e8bcc59-dab1-1b4c-e054-00144ff88e88RxCUI 198014UNII 57Y76R9ATQUPC 0366267153409
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

N466267015310 followed by a unit qualifier and the quantity

Package 66267-0153-10. 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

Current FDA label (SPL), effective Aug 13, 2024. This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Carefully consider the potential benefits and risks of naproxen, naproxen sodium and other treatment options before deciding to use naproxen tablets or naproxen sodium tablets. Use the lowest effective dosage for the shortest duration consistent with individual patient treatment goals (see WARNINGS: Gastrointestinal Bleeding, Ulceration, and Perforation ). Naproxen as naproxen tablets or naproxen sodium 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 arth…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 66267-153

What is NDC 66267-153?: 66267-153 is the product NDC for Naproxen, Naproxen 500 mg/1 tablet, listed with the FDA by NuCare Pharmaceuticals, Inc.. It has 9 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?: NuCare Pharmaceuticals, Inc., NDC labeler code 66267. 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?: 189 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	Unit Dose Solutions, Inc.	87441-092	87441-0092-01
Naproxen	Naproxen 500 mg/1	TabletOral	St. Mary's Medical Park Pharmacy	60760-190	60760-0190-60
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

All 190 Naproxen NDCs

Other NDCs under ANDA 078250

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

FDA NDC Directory listings under ANDA 078250
Product	Strength	Form · route	Labeler	Product NDC
Naproxen	Naproxen 500 mg/1	TabletOral	A-S Medication Solutions	50090-0481
Naproxen	Naproxen 500 mg/1	TabletOral	A-S Medication Solutions	50090-0482
Naproxen	Naproxen 500 mg/1	TabletOral	A-S Medication Solutions	50090-0483
Naproxen	Naproxen 375 mg/1	TabletOral	A-S Medication Solutions	50090-1583
Naproxen	Naproxen 375 mg/1	TabletOral	A-S Medication Solutions	50090-1584
Naproxen	Naproxen 375 mg/1	TabletOral	A-S Medication Solutions	50090-1585
Naproxen	Naproxen 250 mg/1	TabletOral	A-S Medication Solutions	50090-2788
Naproxen	Naproxen 500 mg/1	TabletOral	A-S Medication Solutions	50090-7198
Naproxen	Naproxen 500 mg/1	TabletOral	American Health Packaging	60687-491
Naproxen	Naproxen 500 mg/1	TabletOral	St. Mary's Medical Park Pharmacy	60760-190
Naproxen	Naproxen 500 mg/1	TabletOral	Proficient Rx LP	63187-028
Naproxen	Naproxen 250 mg/1	TabletOral	Proficient Rx LP	63187-461
Naproxen	Naproxen 375 mg/1	TabletOral	Proficient Rx LP	63187-535
Naproxen	Naproxen 500 mg/1	TabletOral	NuCare Pharmaceuticals, Inc.	66267-807
Naproxen	Naproxen 250 mg/1	TabletOral	Coupler LLC	67046-0499
Naproxen	Naproxen 375 mg/1	TabletOral	Coupler LLC	67046-0500
Naproxen	Naproxen 500 mg/1	TabletOral	Coupler LLC	67046-0501
Naproxen	Naproxen 250 mg/1	TabletOral	Glenmark Pharmaceuticals Inc., USA	68462-188
Naproxen	Naproxen 375 mg/1	TabletOral	Glenmark Pharmaceuticals Inc., USA	68462-189
Naproxen	Naproxen 500 mg/1	TabletOral	Glenmark Pharmaceuticals Inc., USA	68462-190

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