What is NDC 79481-0183?

79481-0183 is the product NDC for Acetaminophen, Acetaminophen 650 mg/1 tablet, listed with the FDA by MEIJER DISTRIBUTION INC. It has 4 package NDCs, shown above in 10- and 11-digit form.

MEIJER DISTRIBUTION INC, NDC labeler code 79481. 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 79481-0183 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)79481-0183Labeler and product segments. Claims need a package NDC.

Product NDC at billing width79481-0183Add 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
79481-0183-1	7948101830179481018301	100 TABLET in 1 BOTTLE (79481-0183-1)Marketed from Jul 17, 2023
79481-0183-2	7948101830279481018302	225 TABLET in 1 BOTTLE (79481-0183-2)Marketed from Jul 17, 2023
79481-0183-4	7948101830479481018304	400 TABLET in 1 BOTTLE (79481-0183-4)Marketed from Jul 17, 2023
79481-0183-5	7948101830579481018305	150 TABLET in 1 BOTTLE (79481-0183-5)Marketed from Jul 17, 2023

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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
Route: Oral
Labeler: MEIJER DISTRIBUTION INCNDC labeler code 79481
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 211544
Marketing start: Jul 17, 2023
Listing expires: Dec 31, 2026
Identifiers: Product ID 79481-0183_46512232-be54-7eef-e063-6294a90a925eSPL ID 46512232-be54-7eef-e063-6294a90a925eSPL set ID ed23c587-7806-1f64-e053-2a95a90aea7fRxCUI 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

N479481018301 followed by a unit qualifier and the quantity

Package 79481-0183-01. 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 Dec 19, 2025.

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 79481-0183

What is NDC 79481-0183?: 79481-0183 is the product NDC for Acetaminophen, Acetaminophen 650 mg/1 tablet, listed with the FDA by MEIJER DISTRIBUTION INC. It has 4 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?: MEIJER DISTRIBUTION INC, NDC labeler code 79481. 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	Tablet, Film coatedOral	Amazon.com Services LLC	72288-099	72288-0099-79
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	Family Dollar, Inc.	55319-751	55319-0751-24
Acetaminophen	Acetaminophen 500 mg/1	TabletOral	PUBLIX SUPERMARKETS, INC	41415-175	41415-0175-0541415-0175-10

All 235 Acetaminophen NDCs

Other NDCs under ANDA 211544

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

FDA NDC Directory listings under ANDA 211544
Product	Strength	Form · route	Labeler	Product NDC
Acetaminophen	Acetaminophen 650 mg/1	Tablet, Extended releaseOral	Bi-Mart	37835-512
Arthritis Pain Reliefacetaminophen	Acetaminophen 650 mg/1	Tablet, Extended releaseOral	TOPCO ASSOCIATES LLC	36800-632
Acetaminophen	Acetaminophen 650 mg/1	Tablet, Film coated, Extended releaseOral	CVS PHARMACY iNC	69842-297
Arthritis Painacetaminophen	Acetaminophen 650 mg/1	Tablet, Extended releaseOral	AAA Pharmaceutical, Inc.	57344-200
8HR Muscle Aches and Painacetaminophen	Acetaminophen 650 mg/1	Tablet, Extended releaseOral	AAA Pharmaceutical, Inc.	57344-201
8 Hour Pain Reliefacetaminophen	Acetaminophen 650 mg/1	Tablet, Extended releaseOral	CHAIN DRUG MARKETING ASSOCIATION, INC.	83324-082
8 Hour Arthritis Painacetaminophen	Acetaminophen 650 mg/1	Tablet, Extended releaseOral	CHAIN DRUG MARKETING ASSOCIATION, INC.	83324-083
Acetaminophen	Acetaminophen 650 mg/1	Tablet, Film coated, Extended releaseOral	WALGREENS	0363-9992
Acetaminophen	Acetaminophen 650 mg/1	Tablet, Film coated, Extended releaseOral	CVS PHARMACY INC	69842-322
Acetaminophen	Acetaminophen 650 mg/1	Tablet, Extended releaseOral	Granules India Limited	62207-188
Acetaminophen	Acetaminophen 650 mg/1	Tablet, Extended releaseOral	Granules India Limited	62207-183
Acetaminophen	Acetaminophen 650 mg/1	TabletOral	MAJOR PHARMACEUTICALS	0904-7314
Acetaminophen	Acetaminophen 650 mg/1	TabletOral	SAM'S WEST INC	68196-935
Acetaminophen	Acetaminophen 650 mg/1	Tablet, Extended releaseOral	Granules Pharmaceuticals Inc.	70010-160
8HR Arthritis Painacetaminophen	Acetaminophen 650 mg/1	Tablet, Extended releaseOral	Demoulas Super Markets, Inc	53942-200
Acetaminophen	Acetaminophen 650 mg/1	Tablet, Film coated, Extended releaseOral	WAL-MART STORES INC	49035-181
GoodMeds Acetaminophen Extended Releaseacetaminophen extended release	Acetaminophen 650 mg/1	Tablet, Extended releaseOral	Cabinet Health P.B.C.	82725-4054
Acetaminophen	Acetaminophen 650 mg/1	Tablet, Extended releaseOral	Bryant Ranch Prepack	71335-1340
Pain Relief (Arthritis)	Acetaminophen 650 mg/1	Tablet, Film coated, Extended releaseOral	Demoulas Super Markets, Inc.	53942-461
DOLO - NeuroBion Acetaminophen Max Extended-Release 650 mgacetaminophen	Acetaminophen 650 mg/1	TabletOral	BENARD INDUSTRIES INC	55959-179

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