What is NDC 69842-322?

69842-322 is the product NDC for Acetaminophen, Acetaminophen 650 mg/1 tablet, film coated, extended release, listed with the FDA by CVS PHARMACY INC. It has 2 package NDCs, shown above in 10- and 11-digit form.

CVS PHARMACY INC, NDC labeler code 69842. 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 69842-322 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)69842-322Labeler and product segments. Claims need a package NDC.

Product NDC at billing width69842-0322Add 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
69842-322-10	6984203221069842032210	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69842-322-10)Marketed from Feb 1, 2021
69842-322-24	6984203222469842032224	24 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69842-322-24)Marketed from Feb 1, 2021

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, Film coated, Extended release
Route: Oral
Labeler: CVS PHARMACY INCNDC labeler code 69842
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 211544
Marketing start: Feb 1, 2021
Listing expires: Dec 31, 2026
Identifiers: Product ID 69842-322_46a0f3f6-a3db-49b3-e063-6294a90ad1c7SPL ID 46a0f3f6-a3db-49b3-e063-6294a90ad1c7SPL set ID bd8ce39f-ccf8-3976-e053-2a95a90abb1fRxCUI 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

N469842032210 followed by a unit qualifier and the quantity

Package 69842-0322-10. 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 23, 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 69842-322

What is NDC 69842-322?: 69842-322 is the product NDC for Acetaminophen, Acetaminophen 650 mg/1 tablet, film coated, extended release, listed with the FDA by CVS PHARMACY INC. It has 2 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?: CVS PHARMACY INC, NDC labeler code 69842. 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 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
Arthritis Painacetaminophen	Acetaminophen 650 mg/1	Tablet, Extended releaseOral	Grocery Outlet, Inc.	85828-200
Acetaminophen	Acetaminophen 650 mg/1	Tablet, Extended releaseOral	Bi-Mart	37835-512
Acetaminophen	Acetaminophen 650 mg/1	TabletOral	Walgreens	0363-0892
Arthritis Pain Reliefacetaminophen	Acetaminophen 650 mg/1	Tablet, Extended releaseOral	TOPCO ASSOCIATES LLC	36800-632
8HR Muscle Aches and Painacetaminophen	Acetaminophen 650 mg/1	Tablet, Extended releaseOral	AAA Pharmaceutical, Inc.	57344-201
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
Acetaminophen	Acetaminophen 650 mg/1	Tablet, Extended releaseOral	Granules India Limited	62207-183
Acetaminophen	Acetaminophen 650 mg/1	Tablet, Extended releaseOral	Granules India Limited	62207-188
Acetaminophen	Acetaminophen 650 mg/1	Tablet, Extended releaseOral	NCS HealthCare of KY, LLC dba Vangard Labs	0615-8624
8 Hour Arthritis Painacetaminophen	Acetaminophen 650 mg/1	Tablet, Extended releaseOral	CHAIN DRUG MARKETING ASSOCIATION, INC.	83324-083
8 Hour Pain Reliefacetaminophen	Acetaminophen 650 mg/1	Tablet, Extended releaseOral	CHAIN DRUG MARKETING ASSOCIATION, INC.	83324-082
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
Acetaminophen	Acetaminophen 650 mg/1	Tablet, Extended releaseOral	Bryant Ranch Prepack	71335-1340
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
Acetaminophen	Acetaminophen 650 mg/1	Tablet, Film coated, Extended releaseOral	WALGREENS	0363-9992
DOLO - NeuroBion Acetaminophen Max Extended-Release 650 mgacetaminophen	Acetaminophen 650 mg/1	TabletOral	BENARD INDUSTRIES INC	55959-179
Acetaminophen	Acetaminophen 650 mg/1	Tablet, Extended releaseOral	Granules India Limited	62207-892

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