What is NDC 0113-8264?

0113-8264 is the product NDC for good sense naproxen sodium, Diphenhydramine hydrochloride 25 mg/1; Naproxen sodium 220 mg/1 tablet, film coated, listed with the FDA by L. Perrigo Company. It has 3 package NDCs, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

good sense naproxen sodium (Diphenhydramine hydrochloride, naproxen sodium).

What is the active ingredient?

Diphenhydramine hydrochloride, Naproxen sodium.

L. Perrigo Company, NDC labeler code 0113. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for good sense naproxen sodium?

6 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

good sense naproxen sodium NDC 0113-8264

NDC codes

FDA NDC Directory

Product NDC (as listed)0113-8264Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00113-8264Add 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
0113-8264-06	0011382640600113826406	1 BOTTLE in 1 CARTON (0113-8264-06) / 160 TABLET, FILM COATED in 1 BOTTLE (0113-8264-00)Marketed from Feb 26, 2026
0113-8264-60	0011382646000113826460	1 BOTTLE in 1 CARTON (0113-8264-60) / 20 TABLET, FILM COATED in 1 BOTTLEMarketed from Dec 28, 2018
0113-8264-71	0011382647100113826471	1 BOTTLE in 1 CARTON (0113-8264-71) / 50 TABLET, FILM COATED in 1 BOTTLEMarketed from Mar 14, 2022

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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): good sense naproxen sodium
Generic name (nonproprietary): diphenhydramine hydrochloride, naproxen sodium
Active ingredients: Diphenhydramine hydrochloride — 25 mg/1Naproxen sodium — 220 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: L. Perrigo CompanyNDC labeler code 0113
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 208499
Marketing start: Dec 28, 2018
Listing expires: Dec 31, 2027
Other FDA classes: Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)Histamine H1 Receptor Antagonists (Mechanism)
Identifiers: Product ID 0113-8264_2d70302c-e43d-4422-a002-57505904f605SPL ID 2d70302c-e43d-4422-a002-57505904f605SPL set ID f548aa3d-b35e-458a-9815-3595a451ab78RxCUI 1550957UNII TC2D6JAD40, 9TN87S3A3C
Pharmacologic class: Histamine-1 Receptor Antagonist; 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

N400113826406 followed by a unit qualifier and the quantity

Package 00113-8264-06. 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 May 11, 2026.

Indications (excerpt from the label)

Uses • for relief of occasional sleeplessness when associated with minor aches and pains • helps you fall asleep and stay asleep

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 0113-8264

What is NDC 0113-8264?: 0113-8264 is the product NDC for good sense naproxen sodium, Diphenhydramine hydrochloride 25 mg/1; Naproxen sodium 220 mg/1 tablet, film coated, listed with the FDA by L. Perrigo Company. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: good sense naproxen sodium (Diphenhydramine hydrochloride, naproxen sodium).
What is the active ingredient?: Diphenhydramine hydrochloride, Naproxen sodium.
Who is the labeler?: L. Perrigo Company, NDC labeler code 0113. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for good sense naproxen sodium?: 6 other product NDCs are listed under this name. See all good sense 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 good sense naproxen sodium NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Good Sense Naproxen Sodiumnaproxen sodium	Naproxen sodium 220 mg/1	Tablet, Film coatedOral	Preferred Pharmaceuticals Inc.	68788-8443	68788-8443-0268788-8443-0368788-8443-04+1 more
good sense naproxen sodiumnaproxen sodium	Naproxen sodium 220 mg/1	Tablet, Film coatedOral	L. Perrigo Company	0113-1412	00113-1412-71
Good Sense Naproxen Sodiumnaproxen sodium	Naproxen sodium 220 mg/1	Tablet, Film coatedOral	L. Perrigo Company	0113-0901	00113-0901-6200113-0901-7100113-0901-75
Good Sense Naproxen Sodiumnaproxen sodium	Naproxen sodium 220 mg/1	Tablet, Film coatedOral	L. Perrigo Company	0113-4368	00113-4368-6200113-4368-7100113-4368-75+2 more
Good Sense Naproxen Sodiumnaproxen sodium	Naproxen sodium 220 mg/1	Tablet, Film coatedOral	Proficient Rx LP	63187-794	63187-0794-2063187-0794-3063187-0794-60
Good Sense Naproxen Sodiumnaproxen sodium	Naproxen sodium 220 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	71335-2584	71335-2584-0171335-2584-0271335-2584-03+6 more

Other NDCs under ANDA 208499

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

FDA NDC Directory listings under ANDA 208499
Product	Strength	Form · route	Labeler	Product NDC
All Night Pain Relief PMdiphenhydramine hydrochloride, naproxen sodium	Diphenhydramine hydrochloride 25 mg/1; Naproxen sodium 220 mg/1	Tablet, Film coatedOral	Walgreen Company	0363-2264
basic care naproxen sodium pmdiphenhydramine hydrochloride, naproxen sodium	Diphenhydramine hydrochloride 25 mg/1; Naproxen sodium 220 mg/1	Tablet, Film coatedOral	Amazon.com Services LLC	72288-310
careone naproxen sodium pmdiphenhydramine hydrochloride, naproxen sodium	Diphenhydramine hydrochloride 25 mg/1; Naproxen sodium 220 mg/1	Tablet, Film coatedOral	American Sales Company	41520-264
dg health naproxen sodium pmdiphenhydramine hydrochloride, naproxen sodium	Diphenhydramine hydrochloride 25 mg/1; Naproxen sodium 220 mg/1	Tablet, Film coatedOral	Dolgencorp Inc	55910-858
equaline naproxen sodium pmdiphenhydramine hydrochloride, naproxen sodium	Diphenhydramine hydrochloride 25 mg/1; Naproxen sodium 220 mg/1	Tablet, Film coatedOral	United Natural Foods, Inc. dba UNFI	41163-593
Naproxen Sodium PMdiphenhydramine hydrochloride, naproxen sodium	Diphenhydramine hydrochloride 25 mg/1; Naproxen sodium 220 mg/1	Tablet, Film coatedOral	Safeway	21130-639
naproxen sodium pmdiphenhydramine hydrochloride, naproxen sodium	Diphenhydramine hydrochloride 25 mg/1; Naproxen sodium 220 mg/1	TabletOral	Kroger Company	30142-753
naproxen sodium pmdiphenhydramine hydrochloride, naproxen sodium	Diphenhydramine hydrochloride 25 mg/1; Naproxen sodium 220 mg/1	Tablet, Film coatedOral	H E B	37808-264
naproxen sodium pmdiphenhydramine hydrochloride, naproxen sodium	Diphenhydramine hydrochloride 25 mg/1; Naproxen sodium 220 mg/1	Tablet, Film coatedOral	Meijer Distribution Inc	41250-526
topcare all night pain relief pmdiphenhydramine hydrochloride, naproxen sodium	Diphenhydramine hydrochloride 25 mg/1; Naproxen sodium 220 mg/1	Tablet, Film coatedOral	Topco Associates LLC	36800-264
up and up naproxen sodium pmdiphenhydramine hydrochloride, naproxen sodium	Diphenhydramine hydrochloride 25 mg/1; Naproxen sodium 220 mg/1	Tablet, Film coatedOral	Target Corporation	11673-687