Acetaminophen Aspirin And Caffeine NDC 58602-882

NDC codes

FDA NDC Directory

Product NDC (as listed)58602-882Labeler and product segments. Claims need a package NDC.

Product NDC at billing width58602-0882Add 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	Copy
58602-882-21	58602088221	1 BOTTLE in 1 CARTON (58602-882-21) / 100 TABLET, FILM COATED in 1 BOTTLEMarketed from Jun 23, 2022
58602-882-38	58602088238	1 BOTTLE in 1 CARTON (58602-882-38) / 300 TABLET, FILM COATED in 1 BOTTLEMarketed from Jun 23, 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): Acetaminophen Aspirin And Caffeine
Generic name (nonproprietary): acetaminophen, aspirin and caffeine
Active ingredients: Acetaminophen — 250 mg/1Aspirin — 250 mg/1Caffeine — 65 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Aurohealth LLC
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 211695
Marketing start: Jun 23, 2022
Listing expires: Dec 31, 2026
Other FDA classes: Non-Steroidal (Chemical structure)Central Nervous System Stimulation (Physiologic effect)Cyclooxygenase Inhibitors (Mechanism)Decreased Platelet Aggregation (Physiologic effect)Decreased Prostaglandin Production (Physiologic effect)Xanthines (Chemical structure)
Identifiers: Product ID 58602-882_20f3adf2-9058-4420-ac3b-1da54420a1d2SPL ID 20f3adf2-9058-4420-ac3b-1da54420a1d2SPL set ID f5465419-1453-4ccc-a517-1fdff1eb3c05RxCUI 308297UNII 362O9ITL9D, R16CO5Y76E, 3G6A5W338E
Pharmacologic class: Central Nervous System Stimulant; Methylxanthine; Nonsteroidal Anti-inflammatory Drug; Platelet Aggregation Inhibitor

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

N458602088221 followed by a unit qualifier and the quantity

Package 58602-0882-21. 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 1, 2023.

Indications (excerpt from the label)

Use treats migraine

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 211695

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

FDA NDC Directory listings under ANDA 211695
Product	Strength	Form · route	Labeler	Product NDC
Acetaminophen Aspirin And Caffeineacetaminophen, aspirin and caffeine	Acetaminophen 250 mg/1 + 2 more ingredients	Tablet, Film coatedOral	Better Living Brands, LLC	21130-074
Acetaminophen Aspirin And Caffeineacetaminophen, aspirin and caffeine	Acetaminophen 250 mg/1 + 2 more ingredients	Tablet, Film coatedOral	Aurohealth LLC	58602-817
Amazon Basic Care Migraine Reliefacetaminophen, aspirin and caffeine	Acetaminophen 250 mg/1 + 2 more ingredients	Tablet, Film coatedOral	Amazon.com Services LLC	72288-376
Acetaminophen Aspirin And Caffeineacetaminophen, aspirin and caffeine	Acetaminophen 250 mg/1 + 2 more ingredients	Tablet, Film coatedOral	WALMART INC.	79903-216