What is NDC 21130-062?

21130-062 is the product NDC for Naproxen, Naproxen sodium 220 mg/1 tablet, listed with the FDA by Safeway, Inc. It has 3 package NDCs, shown above in 10- and 11-digit form.

Safeway, Inc, NDC labeler code 21130. 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 21130-062 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)21130-062Labeler and product segments. Claims need a package NDC.

Product NDC at billing width21130-0062Add 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
21130-062-05	2113000620521130006205	50 TABLET in 1 BOTTLE (21130-062-05)Marketed from Aug 30, 2023
21130-062-09	2113000620921130006209	90 TABLET in 1 BOTTLE (21130-062-09)Marketed from Aug 30, 2023
21130-062-20	2113000622021130006220	200 TABLET in 1 BOTTLE (21130-062-20)Marketed from Sep 30, 2023

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 sodium — 220 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Safeway, IncNDC labeler code 21130
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 091353
Marketing start: Aug 30, 2023
Listing expires: Dec 31, 2026
Other FDA classes: Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers: Product ID 21130-062_4650a28b-d299-a5e5-e063-6294a90ad9f7SPL ID 4650a28b-d299-a5e5-e063-6294a90ad9f7SPL set ID f2a273f8-d623-dc2f-e053-2995a90a0c02RxCUI 849574UNII 9TN87S3A3C
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

N421130006205 followed by a unit qualifier and the quantity

Package 21130-0062-05. 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 19, 2025.

Indications (excerpt from the label)

Uses ■ temporarily relieves minor aches and pains due to: ■ minor pain of arthritis ■ muscular aches ■ backache ■ mentrual cramps ■ headache ■ toothache ■ the common cold ■ temporarily reduces fever

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 21130-062

What is NDC 21130-062?: 21130-062 is the product NDC for Naproxen, Naproxen sodium 220 mg/1 tablet, listed with the FDA by Safeway, Inc. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Naproxen.
What is the active ingredient?: Naproxen sodium.
Who is the labeler?: Safeway, Inc, NDC labeler code 21130. 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 091353

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

FDA NDC Directory listings under ANDA 091353
Product	Strength	Form · route	Labeler	Product NDC
Pain Reliefnaproxen sodium	Naproxen sodium 220 mg/1	Tablet, Film coatedOral	Gobrands, Inc	82501-1576
All Day Pain Reliefnaproxen sodium tablets, 220 mg	Naproxen sodium 220 mg/1	TabletOral	HealthLife of USA LLC	69517-109
Dr Simi All Day Pain Reliefnaproxen sodium	Naproxen sodium 220 mg/1	Tablet, Film coatedOral	Farmacias De Similares TX LLC	85786-104
Naproxen Sodium	Naproxen sodium 220 mg/1	TabletOral	TARGET CORPORATION	11673-764
Naproxen Sodium	Naproxen sodium 220 mg/1	TabletOral	Safeway, Inc	21130-061
Naproxen Sodium	Naproxen sodium 220 mg/1	TabletOral	Bi-Mart	37835-594
Naproxen Sodium	Naproxen sodium 220 mg/1	TabletOral	Granules India Ltd	62207-327
Naproxen Sodium	Naproxen sodium 220 mg/1	TabletOral	Granules India Ltd	62207-328
Naproxen Sodium	Naproxen sodium 220 mg/1	TabletOral	CVS	51316-761
Naproxen Sodium	Naproxen sodium 220 mg/1	TabletOral	CVS	51316-762
Naproxen Sodium	Naproxen sodium 220 mg/1	TabletOral	Granules India Ltd	62207-728
Naproxen Sodium	Naproxen sodium 220 mg/1	TabletOral	Granules India Ltd	62207-729
Naproxen Sodium	Naproxen sodium 220 mg/1	Tablet, Film coated, Extended releaseOral	SPIRIT PHARMACEUTICALS,LLC	68210-4096
Rapidol Naproxennaproxen sodium	Naproxen sodium 220 mg/1	Tablet, CoatedOral	Pharmadel LLC	55758-048
Naproxen Sodium	Naproxen sodium 220 mg/1	Tablet, Film coatedOral	Granules India Ltd	62207-761
Naproxen Sodium	Naproxen sodium 220 mg/1	Tablet, Film coatedOral	Granules India Ltd	62207-762
Proxen Np 660naproxen sodium	Naproxen sodium 220 mg/1	TabletOral	OPMX LLC	69729-123
Naproxen Sodium	Naproxen sodium 220 mg/1	TabletOral	Granules USA, Inc.	69848-010