What is NDC 58602-730?

58602-730 is the product NDC for Acetaminophen, Acetaminophen 650 mg/1 tablet, extended release, listed with the FDA by Aurohealth LLC. It has 14 package NDCs, shown above in 10- and 11-digit form.

Aurohealth LLC, NDC labeler code 58602. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Acetaminophen?

234 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Acetaminophen NDC 58602-730 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)58602-730Labeler and product segments. Claims need a package NDC.

Product NDC at billing width58602-0730Add 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
58602-730-07	5860207300758602073007	1 BOTTLE in 1 CARTON (58602-730-07) / 24 TABLET, EXTENDED RELEASE in 1 BOTTLEMarketed from Aug 11, 2018
58602-730-14	5860207301458602073014	1 BOTTLE in 1 CARTON (58602-730-14) / 50 TABLET, EXTENDED RELEASE in 1 BOTTLEMarketed from Aug 11, 2018
58602-730-21	5860207302158602073021	1 BOTTLE in 1 CARTON (58602-730-21) / 100 TABLET, EXTENDED RELEASE in 1 BOTTLEMarketed from Aug 11, 2018
58602-730-28	5860207302858602073028	1 BOTTLE in 1 CARTON (58602-730-28) / 225 TABLET, EXTENDED RELEASE in 1 BOTTLEMarketed from Dec 29, 2021
58602-730-29	5860207302958602073029	150 TABLET, EXTENDED RELEASE in 1 BOTTLE (58602-730-29)Marketed from Aug 11, 2018
58602-730-34	5860207303458602073034	200 TABLET, EXTENDED RELEASE in 1 BOTTLE (58602-730-34)Marketed from Aug 11, 2018
58602-730-35	5860207303558602073035	225 TABLET, EXTENDED RELEASE in 1 BOTTLE (58602-730-35)Marketed from Aug 11, 2018
58602-730-36	5860207303658602073036	1 BOTTLE in 1 CARTON (58602-730-36) / 250 TABLET, EXTENDED RELEASE in 1 BOTTLEMarketed from Nov 9, 2016
58602-730-40	5860207304058602073040	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (58602-730-40)Marketed from Aug 11, 2018
58602-730-41	5860207304158602073041	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (58602-730-41)Marketed from Aug 11, 2018
58602-730-44	5860207304458602073044	400 TABLET, EXTENDED RELEASE in 1 BOTTLE (58602-730-44)Marketed from Jan 11, 2021
58602-730-67	5860207306758602073067	290 TABLET, EXTENDED RELEASE in 1 BOTTLE (58602-730-67)Marketed from Aug 11, 2018
58602-730-76	5860207307658602073076	325 TABLET, EXTENDED RELEASE in 1 BOTTLE (58602-730-76)Marketed from Aug 11, 2018
58602-730-94	5860207309458602073094	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (58602-730-94)Marketed from Apr 8, 2020

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): Acetaminophen
Generic name (nonproprietary): acetaminophen
Active ingredients: Acetaminophen — 650 mg/1
Dosage form: Tablet, Extended release
Route: Oral
Labeler: Aurohealth LLCNDC labeler code 58602
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 207229
Marketing start: Nov 9, 2016
Listing expires: Dec 31, 2027
Identifiers: Product ID 58602-730_462dae43-f3b8-4f6c-846b-de19a01d169cSPL ID 462dae43-f3b8-4f6c-846b-de19a01d169cSPL set ID 179c221d-c099-400c-b3ac-124e26947620RxCUI 1148399UNII 362O9ITL9D

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

N458602073007 followed by a unit qualifier and the quantity

Package 58602-0730-07. 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 Jan 24, 2024.

Indications (excerpt from the label)

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

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 58602-730

What is NDC 58602-730?: 58602-730 is the product NDC for Acetaminophen, Acetaminophen 650 mg/1 tablet, extended release, listed with the FDA by Aurohealth LLC. It has 14 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Acetaminophen.
What is the active ingredient?: Acetaminophen.
Who is the labeler?: Aurohealth LLC, NDC labeler code 58602. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Acetaminophen?: 234 other product NDCs are listed under this name. See all Acetaminophen 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 Acetaminophen NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
acetaminophen	Acetaminophen 500 mg/1	TabletOral	REMEDYREPACK INC.	70518-4787	70518-4787-00
Acetaminophen	Acetaminophen 325 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4782	70518-4782-0070518-4782-01
Acetaminophen	Acetaminophen 500 mg/1	TabletOral	REMEDYREPACK INC.	70518-4783	70518-4783-00
Acetaminophen	Acetaminophen 500 mg/1	TabletOral	Amazon.com Services LLC	72288-440	72288-0440-09
acetaminophen	Acetaminophen 650 mg/1	Tablet, Film coated, Extended releaseOral	Amazon.com Services LLC	72288-150	72288-0150-79
Acetaminophen	Acetaminophen 10 mg/mL	Injection, SolutionIntravenous	Somerset Therapeutics, LLC	70069-871	70069-0871-10
Acetaminophen	Acetaminophen 500 mg/1	TabletOral	Walgreens	0363-9810	00363-9810-1000363-9810-2500363-9810-50+1 more
Acetaminophen	Acetaminophen 500 mg/1	TabletOral	PUBLIX SUPERMARKETS, INC	41415-175	41415-0175-0541415-0175-10
Acetaminophen	Acetaminophen 500 mg/1	TabletOral	Family Dollar, Inc.	55319-751	55319-0751-24
Acetaminophen	Acetaminophen 500 mg/1	TabletOral	Meijer Distribution Inc	79481-0780	79481-0780-0179481-0780-0279481-0780-04

All 235 Acetaminophen NDCs

Other NDCs under ANDA 207229

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

FDA NDC Directory listings under ANDA 207229
Product	Strength	Form · route	Labeler	Product NDC
Acetaminophen	Acetaminophen 650 mg/1	TabletOral	BluePoint Laboratories	68001-495
Acetaminophen	Acetaminophen 650 mg/1	TabletOral	American Health Packaging	60687-924
Acetaminophen	Acetaminophen 650 mg/1	Tablet, Extended releaseOral	WALGREEN CO.	0363-9604
Acetaminophen	Acetaminophen 650 mg/1	Tablet, Extended releaseOral	Better Living Brands, LLC	21130-108
Acetaminophen	Acetaminophen 650 mg/1	Tablet, Extended releaseOral	CVS Pharmacy, Inc.	69842-037
Acetaminophen	Acetaminophen 650 mg/1	Tablet, Extended releaseOral	CVS Pharmacy, Inc.	69842-635
Amazon Basic Care Acetaminophenacetaminophen	Acetaminophen 650 mg/1	Tablet, Extended releaseOral	Amazon.com Services LLC	72288-698
Acetaminophen	Acetaminophen 650 mg/1	Tablet, Extended releaseOral	WALMART INC.	79903-132
Acetaminophen	Acetaminophen 650 mg/1	Tablet, Extended releaseOral	Aurohealth LLC	58602-848
Acetaminophen	Acetaminophen 650 mg/1	Tablet, Extended releaseOral	Aurohealth LLC	58602-873
Acetaminophen	Acetaminophen 650 mg/1	Tablet, Extended releaseOral	KROGER COMPANY	30142-157