What is NDC 69729-123?

69729-123 is the product NDC for Proxen Np 660 (naproxen sodium), Naproxen sodium 220 mg/1 tablet, listed with the FDA by OPMX LLC. It has 3 package NDCs, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Proxen Np 660 (Naproxen Sodium).

OPMX LLC, NDC labeler code 69729. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Proxen Np 660?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Proxen Np 660 NDC 69729-123 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)69729-123Labeler and product segments. Claims need a package NDC.

Product NDC at billing width69729-0123Add 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
69729-123-12	6972901231269729012312	1 BLISTER PACK in 1 CARTON (69729-123-12) / 12 TABLET in 1 BLISTER PACKMarketed from Nov 7, 2023
69729-123-24	6972901232469729012324	2 BLISTER PACK in 1 CARTON (69729-123-24) / 12 TABLET in 1 BLISTER PACKMarketed from Nov 16, 2023
69729-123-50	6972901235069729012350	50 POUCH in 1 CARTON (69729-123-50) / 2 TABLET in 1 POUCHMarketed from Nov 7, 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): Proxen Np 660
Generic name (nonproprietary): naproxen sodium
Active ingredients: Naproxen sodium — 220 mg/1
Dosage form: Tablet
Route: Oral
Labeler: OPMX LLCNDC labeler code 69729
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 091353
Marketing start: Nov 7, 2023
Listing expires: Dec 31, 2026
Other FDA classes: Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers: Product ID 69729-123_0d811063-82c1-bf9f-e063-6294a90aa371SPL ID 0d811063-82c1-bf9f-e063-6294a90aa371SPL set ID 09990b2f-202e-b4df-e063-6394a90a055bRxCUI 849574UNII 9TN87S3A3CUPC 0810053181362, 0810053181379, 0810053181423
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

N469729012312 followed by a unit qualifier and the quantity

Package 69729-0123-12. 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 27, 2023.

Indications (excerpt from the label)

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

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 69729-123

What is NDC 69729-123?: 69729-123 is the product NDC for Proxen Np 660 (naproxen sodium), Naproxen sodium 220 mg/1 tablet, listed with the FDA by OPMX LLC. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Proxen Np 660 (Naproxen Sodium).
What is the active ingredient?: Naproxen sodium.
Who is the labeler?: OPMX LLC, NDC labeler code 69729. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Proxen Np 660?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

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
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	Naproxen sodium 220 mg/1	TabletOral	Safeway, Inc	21130-062
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	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	62207-327
Naproxen Sodium	Naproxen sodium 220 mg/1	TabletOral	Granules India Ltd	62207-328
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 coatedOral	Granules India Ltd	62207-761
Naproxen Sodium	Naproxen sodium 220 mg/1	Tablet, Film coatedOral	Granules India Ltd	62207-762
Naproxen Sodium	Naproxen sodium 220 mg/1	Tablet, Film coated, Extended releaseOral	SPIRIT PHARMACEUTICALS,LLC	68210-4096
Naproxen Sodium	Naproxen sodium 220 mg/1	TabletOral	Granules USA, Inc.	69848-010
Pain Reliefnaproxen sodium	Naproxen sodium 220 mg/1	Tablet, Film coatedOral	Gobrands, Inc	82501-1576
Rapidol Naproxennaproxen sodium	Naproxen sodium 220 mg/1	Tablet, CoatedOral	Pharmadel LLC	55758-048

Proxen Np 660 (Naproxen sodium) NDC 69729-123