What is NDC 36800-770?

36800-770 is the product NDC for Pain Relief Extra Strength (acetaminophen), Acetaminophen 500 mg/1 tablet, coated, listed with the FDA by TopCo Associates LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Pain Relief Extra Strength (Acetaminophen).

TopCo Associates LLC, NDC labeler code 36800. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Pain Relief Extra Strength?

31 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Pain Relief Extra Strength NDC 36800-770

NDC codes

FDA NDC Directory

Product NDC (as listed)36800-770Labeler and product segments. Claims need a package NDC.

Product NDC at billing width36800-0770Add 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
36800-770-02	36800077002	1 BOTTLE, PLASTIC in 1 CARTON (36800-770-02) / 50 TABLET, COATED in 1 BOTTLE, PLASTICMarketed from Mar 31, 2014

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): Pain Relief Extra StrengthSuffix: Extra Strength
Generic name (nonproprietary): acetaminophen
Active ingredients: Acetaminophen — 500 mg/1
Dosage form: Tablet, Coated
Route: Oral
Labeler: TopCo Associates LLCNDC labeler code 36800
Product type: Over-the-counter drug
Marketing category: OTC monograph drugApplication M 013
Marketing start: Mar 31, 2014
Listing expires: Dec 31, 2026
Identifiers: Product ID 36800-770_286014c1-2183-fc25-e063-6394a90aa15eSPL ID 286014c1-2183-fc25-e063-6394a90aa15eSPL set ID ecd6df7e-e7e2-446b-85ef-25971281fe31RxCUI 198440UNII 362O9ITL9DUPC 0036800199903

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

N436800077002 followed by a unit qualifier and the quantity

Package 36800-0770-02. 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 3, 2024.

Indications (excerpt from the label)

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

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 36800-770

What is NDC 36800-770?: 36800-770 is the product NDC for Pain Relief Extra Strength (acetaminophen), Acetaminophen 500 mg/1 tablet, coated, listed with the FDA by TopCo Associates LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Pain Relief Extra Strength (Acetaminophen).
What is the active ingredient?: Acetaminophen.
Who is the labeler?: TopCo Associates LLC, NDC labeler code 36800. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Pain Relief Extra Strength?: 31 other product NDCs are listed under this name. See all Pain Relief Extra Strength 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 Pain Relief Extra Strength NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Pain Relief Extra Strengthacetaminophen	Acetaminophen 500 mg/1	Tablet, CoatedOral	CHAIN DRUG MARKETING ASSOCIATION, INC.	83324-079	83324-0079-50
Pain Relief Extra Strengthacetaminophen	Acetaminophen 500 mg/1	TabletOral	Chain Drug Marketing Association	83324-081	83324-0081-0183324-0081-1083324-0081-60
Pain Relief Extra Strengthacetaminophen	Acetaminophen 500 mg/1	Tablet, CoatedOral	CHAIN DRUG MARKETING ASSOCIATION, INC.	83324-078	83324-0078-0183324-0078-0583324-0078-15+2 more
Pain Relief Extra Strengthacetaminophen	Acetaminophen 500 mg/1	Tablet, CoatedOral	CHAIN DRUG MARKETING ASSOCIATION, INC.	83324-080	83324-0080-01
Pain Relief Extra Strengthacetaminophen	Acetaminophen 500 mg/1	Tablet, CoatedOral	STRATEGIC SOURCING SERVICES LLC	70677-1120	70677-1120-0170677-1120-02
Pain Relief Extra Strengthacetaminophen	Acetaminophen 500 mg/1	TabletOral	STRATEGIC SOURCING SERVICES LLC	70677-1124	70677-1124-01
Pain Relief Extra Strengthacetaminophen	Acetaminophen 500 mg/1	Tablet, CoatedOral	MARC GLASSMAN, INC.	68998-104	68998-0104-0468998-0104-06
Pain Relief Extra Strengthacetaminophen	Acetaminophen 500 mg/1	Tablet, CoatedOral	MARC GLASSMAN, INC.	68998-198	68998-0198-02
Pain Relief Extra Strengthacetaminophen	Acetaminophen 500 mg/1	Tablet, CoatedOral	MARC GLASSMAN, INC.	68998-392	68998-0392-01
Pain Relief Extra Strengthacetaminophen	Acetaminophen 500 mg/1	TabletOral	DISCOUNT DRUG MART	53943-103	53943-0103-0253943-0103-04

All 32 Pain Relief Extra Strength 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
365 whole foods market acetaminophenacetaminophen	Acetaminophen 500 mg/1	TabletOral	Whole Foods Market, INC.	42681-0025
Acetaminophen	Acetaminophen 160 mg/5mL	SolutionOral	PAI Holdings, LLC dba PAI Pharma	0121-0657
Acetaminophen	Acetaminophen 160 mg/5mL	SuspensionOral	PAI Holdings, LLC dba PAI Pharma	0121-0941
Acetaminophen	Acetaminophen 160 mg/5mL	SolutionOral	PAI Holdings, LLC dba PAI Pharma	0121-1047
Acetaminophen	Acetaminophen 325 mg/10.15mL	SolutionOral	PAI Holdings, LLC dba PAI Pharma	0121-1314
Acetaminophen	Acetaminophen 325 mg/10.15mL	SuspensionOral	PAI Holdings, LLC dba PAI Pharma	0121-1882
Acetaminophen	Acetaminophen 650 mg/20.3mL	SolutionOral	PAI Holdings, LLC dba PAI Pharma	0121-1971
Acetaminophen	Acetaminophen 325 mg/10.15mL	SolutionOral	PAI Holdings, LLC dba PAI Pharma	0121-2094
Acetaminophen	Acetaminophen 650 mg/20.3mL	SuspensionOral	PAI Holdings, LLC dba PAI Pharma	0121-2823
Acetaminophen	Acetaminophen 650 mg/20.3mL	SolutionOral	PAI Holdings, LLC dba PAI Pharma	0121-3141
Acetaminophen	Acetaminophen 500 mg/1	TabletOral	WALGREENS	0363-9538
Acetaminophen	Acetaminophen 500 mg/1	TabletOral	WALGREEN CO.	0363-9595
Acetaminophen	Acetaminophen 160 mg/1	TabletOral	WALGREEN CO.	0363-9605
Acetaminophen	Acetaminophen 500 mg/1	TabletOral	WALGREEN CO.	0363-9798
Acetaminophen	Acetaminophen 500 mg/1	TabletOral	Walgreens	0363-9810
Acetaminophen	Acetaminophen 500 mg/1	TabletOral	Rugby Laboratories	0536-1172
Acetaminophen	Acetaminophen 500 mg/1	Tablet, CoatedOral	Rugby Laboratories	0536-1292
Acetaminophen	Acetaminophen 500 mg/1	Tablet, Film coatedOral	Rugby Laboratories	0536-1413
Acetaminophen	Acetaminophen 325 mg/1	Tablet, Film coatedOral	NCS HealthCare of KY, LLC dba Vangard Labs	0615-8608
Acetaminophen	Acetaminophen 325 mg/1	Tablet, Film coatedOral	NCS HealthCare of KY, LLC dba Vangard Labs	0615-8609

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Pain Relief Extra Strength (Acetaminophen) NDC 36800-770

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About NDC 36800-770

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About NDC 36800-770

Related NDCs: other Pain Relief Extra Strength products

Other NDCs under M 013