What is NDC 69230-329?

69230-329 is the product NDC for Naproxen sodium, Naproxen sodium 220 mg/1 tablet, film coated, listed with the FDA by Camber Consumer Care Inc. It has 6 package NDCs, shown above in 10- and 11-digit form.

Camber Consumer Care Inc, NDC labeler code 69230. 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 sodium?

144 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Naproxen sodium NDC 69230-329 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)69230-329Labeler and product segments. Claims need a package NDC.

Product NDC at billing width69230-0329Add 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
69230-329-01	6923003290169230032901	1 BOTTLE in 1 CARTON (69230-329-01) / 100 TABLET, FILM COATED in 1 BOTTLEMarketed from Oct 28, 2022
69230-329-02	6923003290269230032902	1 BOTTLE in 1 CARTON (69230-329-02) / 200 TABLET, FILM COATED in 1 BOTTLEMarketed from Oct 28, 2022
69230-329-05	6923003290569230032905	500 TABLET, FILM COATED in 1 BOTTLE (69230-329-05)Marketed from Oct 28, 2022
69230-329-10	6923003291069230032910	1000 TABLET, FILM COATED in 1 BOTTLE (69230-329-10)Marketed from Oct 28, 2022
69230-329-24	6923003292469230032924	1 BOTTLE in 1 CARTON (69230-329-24) / 24 TABLET, FILM COATED in 1 BOTTLEMarketed from Oct 28, 2022
69230-329-50	6923003295069230032950	1 BOTTLE in 1 CARTON (69230-329-50) / 50 TABLET, FILM COATED in 1 BOTTLEMarketed from Oct 28, 2022

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, Film coated
Route: Oral
Labeler: Camber Consumer Care IncNDC labeler code 69230
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 211065
Marketing start: Oct 28, 2022
Listing expires: Dec 31, 2027
Other FDA classes: Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers: Product ID 69230-329_ee21e0f7-9f32-6c63-e053-2a95a90ac996SPL ID ee21e0f7-9f32-6c63-e053-2a95a90ac996SPL set ID d1008e19-ff0d-4ed2-909d-bae5a82a1234RxCUI 849574UNII 9TN87S3A3CUPC 0369230329016
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

N469230032901 followed by a unit qualifier and the quantity

Package 69230-0329-01. 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 Nov 23, 2022.

Indications (excerpt from the label)

USE(S) • temporarily relieves minor aches and pains due to: • minor pain of arthritis • muscular aches • backache • headache • the common cold • menstrual cramps • toothache • temporarily reduces fever

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 69230-329

What is NDC 69230-329?: 69230-329 is the product NDC for Naproxen sodium, Naproxen sodium 220 mg/1 tablet, film coated, listed with the FDA by Camber Consumer Care Inc. It has 6 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Naproxen sodium.
What is the active ingredient?: Naproxen sodium.
Who is the labeler?: Camber Consumer Care Inc, NDC labeler code 69230. 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 sodium?: 144 other product NDCs are listed under this name. See all Naproxen sodium 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 sodium NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
naproxen sodium	Naproxen sodium 220 mg/1	Tablet, Film coatedOral	Amazon.com Services LLC	72288-988	72288-0988-75
Naproxen Sodium	Naproxen sodium 220 mg/1	Tablet, CoatedOral	AAA Pharmaceutical, Inc.	57344-244	57344-0244-03
Naproxen Sodium	Naproxen sodium 550 mg/1	TabletOral	Advanced Rx of Tennessee, LLC	80425-0574	80425-0574-0180425-0574-0280425-0574-03
Naproxen Sodium	Naproxen sodium 220 mg/1	Tablet, CoatedOral	HYVEE INC	42507-245	42507-0245-0142507-0245-0842507-0245-14
Naproxen Sodium	Naproxen sodium 220 mg/1	Tablet, CoatedOral	HYVEE INC	42507-844	42507-0844-0142507-0844-14
Naproxen Sodium	Naproxen sodium 220 mg/1	Capsule, Liquid filledOral	TARGET Corporation	11673-651	11673-0651-78
Naproxen Sodium	Naproxen sodium 220 mg/1	Tablet, Film coatedOral	Safeway	21130-593	21130-0593-79
Naproxen Sodium	Naproxen sodium 550 mg/1	TabletOral	Advanced Rx of Tennessee, LLC	80425-0531	80425-0531-0180425-0531-0280425-0531-03
Naproxen Sodium	Naproxen sodium 550 mg/1	TabletOral	Advanced Rx of Tennessee, LLC	80425-0532	80425-0532-0180425-0532-0280425-0532-03
Naproxen Sodium	Naproxen sodium 220 mg/1	Tablet, CoatedOral	CHAIN DRUG MARKETING ASSOCIATION, INC.	83324-108	83324-0108-0183324-0108-2483324-0108-50

All 145 Naproxen sodium NDCs