What is NDC 0121-1882?

0121-1882 is the product NDC for Acetaminophen, Acetaminophen 325 mg/10.15mL suspension, listed with the FDA by PAI Holdings, LLC dba PAI Pharma. It has 1 package NDC, shown above in 10- and 11-digit form.

PAI Holdings, LLC dba PAI Pharma, NDC labeler code 0121. 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?

230 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 0121-1882 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)0121-1882Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00121-1882Add 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
0121-1882-00	00121188200	10 TRAY in 1 CASE (0121-1882-00) / 10 CUP, UNIT-DOSE in 1 TRAY / 10.15 mL in 1 CUP, UNIT-DOSE (0121-1882-11)Marketed from Sep 3, 2021

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): Acetaminophen
Generic name (nonproprietary): acetaminophen
Active ingredients: Acetaminophen — 325 mg/10.15mL
Dosage form: Suspension
Route: Oral
Labeler: PAI Holdings, LLC dba PAI PharmaNDC labeler code 0121
Product type: Over-the-counter drug
Marketing category: OTC monograph drugApplication M 013
Marketing start: Sep 3, 2021
Listing expires: Dec 31, 2026
Identifiers: Product ID 0121-1882_bbd6f65a-a6ec-4c17-935c-ed743c45e2c8SPL ID bbd6f65a-a6ec-4c17-935c-ed743c45e2c8SPL set ID caf5daea-409e-5dd2-e053-2995a90acb12RxCUI 307668UNII 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

N400121188200 followed by a unit qualifier and the quantity

Package 00121-1882-00. 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 Aug 18, 2025.

Indications (excerpt from the label)

Uses temporarily: reduces fever relieves minor aches and pains due to: the common cold flu headache sore throat toothache

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 0121-1882

What is NDC 0121-1882?: 0121-1882 is the product NDC for Acetaminophen, Acetaminophen 325 mg/10.15mL suspension, listed with the FDA by PAI Holdings, LLC dba PAI Pharma. It has 1 package NDC, 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?: PAI Holdings, LLC dba PAI Pharma, NDC labeler code 0121. 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?: 230 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 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
Acetaminophen	Acetaminophen 500 mg/1	TabletOral	Meijer Distribution Inc	79481-0780	79481-0780-0179481-0780-0279481-0780-04
Acetaminophen	Acetaminophen 500 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-4132	68788-4132-0168788-4132-0268788-4132-03+1 more
acetaminophen	Acetaminophen 500 mg/1	TabletOral	Unit Dose Solutions, Inc.	87441-008	87441-0008-01
Acetaminophen	Acetaminophen 160 mg/5mL	SolutionOral	Acetris Pharma Holdings, LLC	52343-555	52343-0555-12
Acetaminophen	Acetaminophen 650 mg/1	Tablet, Extended releaseOral	Granules India Limited	62207-892	62207-0892-4962207-0892-51

All 231 Acetaminophen NDCs

Other NDCs under M 013

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

FDA NDC Directory listings under M 013
Product	Strength	Form · route	Labeler	Product NDC
Xesso Neobenzocaine	Benzocaine 5 g/100mL	SprayOral, Topical	PREMIUM NATURAL COSMETICS INC	81777-106
MAX relief junior Grapechildrens acetaminophen	Acetaminophen 160 mg/5mL	LiquidOral	ATLANTIC BIOLOGICALS CORP.	17856-1123
equate aspirinaspirin	Aspirin 81 mg/1	Tablet, ChewableOral	Wal-Mart Stores Inc	49035-467
Acetaminophen	Acetaminophen 325 mg/1	TabletOral	Cardinal Health 107, LLC	55154-7899
Acetaminophen	Acetaminophen 325 mg/1	Tablet, Film coatedOral	Rising Pharma Holdings, Inc.	57237-346
Bayer Rapid Reliefaspirin/caffeine oral powder	Caffeine 65 mg/1; Aspirin 650 mg/1	PowderOral	Bayer HealthCare LLC.	0280-0103
Acetaminophen	Acetaminophen 650 mg/20.3mL	SolutionOral	PAI Holdings, LLC dba PAI Pharma	0121-3141
Headache Reliefacetaminophen, aspirin, caffeine	Acetaminophen 250 mg/1 + 2 more ingredients	Tablet, Film coatedOral	DOLGENCORP, LLC	55910-345
Aspirin Enteric Coated, Regular Strengthaspirin	Aspirin 325 mg/1	Tablet, Delayed releaseOral	Walgreen Company	0363-0227
Aspirin	Aspirin 325 mg/1	Tablet, CoatedOral	CHAIN DRUG MARKETING ASSOCIATION, INC.	83324-205
MAX relief junior Grapechildrens acetaminophen	Acetaminophen 160 mg/5mL	LiquidOral	ATLANTIC BIOLOGICALS CORP.	17856-1122
Pain Relief Extra Strengthacetaminophen	Acetaminophen 500 mg/1	Tablet, CoatedOral	H E B	37808-195
childrens mapapacetaminophen	Acetaminophen 160 mg/1	Tablet, ChewableOral	Proficient Rx LP	71205-322
Acetaminophen	Acetaminophen 500 mg/1	TabletOral	WALMART INC	79903-296
Extra Strength Pain Relieveracetaminophen 500 mg	Acetaminophen 500 mg/1	TabletOral	Lil' Drug Store Products, Inc.	29485-9281
Acetaminophen	Acetaminophen 500 mg/1	TabletOral	Cardinal Health 107, LLC	55154-7897
Headache Formula Extra Strengthacetaminophen, aspirin, caffeine	Acetaminophen 250 mg/1 + 2 more ingredients	Tablet, Film coatedOral	ARMY AND AIR FORCE EXCHANGE SERVICE	55301-334
Acetaminophen	Acetaminophen 500 mg/1	TabletOral	Family Dollar, Inc.	55319-751
Alka-Seltzerbuffered aspirin	Aspirin 325 mg/1	Tablet, EffervescentOral	Lil' Drug Store Products, Inc.	66715-5206
Extra Strength Pain Reliefacetaminophen	Acetaminophen 500 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-8786

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