Over-the-counter drug · OTC MONOGRAPH DRUG

M-Pap (Acetaminophen) NDC 58657-524

Acetaminophen 160 mg/5mL · Liquid · Oral · Method Pharmaceuticals, LLC

NDC codes

FDA NDC Directory
Product NDC (as listed)58657-524Labeler and product segments. Claims need a package NDC.
Product NDC at billing width58657-0524Add 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 NDC11-digit (billing)PackageCopy
58657-524-0458657052404120 mL in 1 BOTTLE (58657-524-04)Marketed from Apr 1, 2024
58657-524-1658657052416473 mL in 1 BOTTLE (58657-524-16)Marketed from Apr 1, 2024

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)
M-Pap
Generic name (nonproprietary)
acetaminophen
Active ingredients
Acetaminophen — 160 mg/5mL
Dosage form
Liquid
Route
Oral
Labeler
Method Pharmaceuticals, LLCNDC labeler code 58657
Product type
Over-the-counter drug
Marketing category
OTC monograph drugApplication M 013
Marketing start
Listing expires
Identifiers
Product ID 58657-524_41b5cace-10a5-04fa-e063-6394a90af9faSPL ID 41b5cace-10a5-04fa-e063-6394a90af9faSPL set ID 1539dc44-15a0-153b-e063-6294a90a9d45RxCUI 307675UNII 362O9ITL9DUPC 0358657524043

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

N458657052404 followed by a unit qualifier and the quantity

Package 58657-0524-04. 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 .

Indications (excerpt from the label)

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

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 58657-524

What is NDC 58657-524?
58657-524 is the product NDC for M-Pap (acetaminophen), Acetaminophen 160 mg/5mL liquid, listed with the FDA by Method Pharmaceuticals, LLC. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
M-Pap (Acetaminophen).
What is the active ingredient?
Acetaminophen.
Who is the labeler?
Method Pharmaceuticals, LLC, NDC labeler code 58657. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for M-Pap?
7 other product NDCs are listed under this name. See all M-Pap 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 M-Pap NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
M-PapacetaminophenAcetaminophen 160 mg/5mLLiquidOralBryant Ranch Prepack71335-275571335-2755-01
M-PapacetaminophenAcetaminophen 160 mg/5mLLiquidOralBryant Ranch Prepack72162-240472162-2404-0272162-2404-04
M-PapacetaminophenAcetaminophen 160 mg/5mLLiquidOralVERITYRX, LLC83939-001183939-0011-0183939-0011-0283939-0011-03+2 more
M-PapacetaminophenAcetaminophen 160 mg/5mLLiquidOralMethod Pharmaceuticals, LLC58657-52558657-0525-0458657-0525-16
M-PapacetaminophenAcetaminophen 160 mg/5mLLiquidOralBryant Ranch Prepack63629-115763629-1157-01
M-PapacetaminophenAcetaminophen 160 mg/5mLLiquidOralBryant Ranch Prepack63629-115863629-1158-01
M-PapacetaminophenAcetaminophen 160 mg/5mLLiquidOralBryant Ranch Prepack72162-167372162-1673-0272162-1673-04

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
ProductStrengthForm · routeLabelerProduct NDC
365 whole foods market acetaminophenacetaminophenAcetaminophen 500 mg/1TabletOralWhole Foods Market, INC.42681-0025
AcetaminophenAcetaminophen 160 mg/5mLSolutionOralPAI Holdings, LLC dba PAI Pharma0121-0657
AcetaminophenAcetaminophen 160 mg/5mLSuspensionOralPAI Holdings, LLC dba PAI Pharma0121-0941
AcetaminophenAcetaminophen 160 mg/5mLSolutionOralPAI Holdings, LLC dba PAI Pharma0121-1047
AcetaminophenAcetaminophen 325 mg/10.15mLSolutionOralPAI Holdings, LLC dba PAI Pharma0121-1314
AcetaminophenAcetaminophen 325 mg/10.15mLSuspensionOralPAI Holdings, LLC dba PAI Pharma0121-1882
AcetaminophenAcetaminophen 650 mg/20.3mLSolutionOralPAI Holdings, LLC dba PAI Pharma0121-1971
AcetaminophenAcetaminophen 325 mg/10.15mLSolutionOralPAI Holdings, LLC dba PAI Pharma0121-2094
AcetaminophenAcetaminophen 650 mg/20.3mLSuspensionOralPAI Holdings, LLC dba PAI Pharma0121-2823
AcetaminophenAcetaminophen 650 mg/20.3mLSolutionOralPAI Holdings, LLC dba PAI Pharma0121-3141
AcetaminophenAcetaminophen 500 mg/1TabletOralWALGREENS0363-9538
AcetaminophenAcetaminophen 500 mg/1TabletOralWALGREEN CO.0363-9595
AcetaminophenAcetaminophen 160 mg/1TabletOralWALGREEN CO.0363-9605
AcetaminophenAcetaminophen 500 mg/1TabletOralWALGREEN CO.0363-9798
AcetaminophenAcetaminophen 500 mg/1TabletOralWalgreens0363-9810
AcetaminophenAcetaminophen 500 mg/1TabletOralRugby Laboratories0536-1172
AcetaminophenAcetaminophen 500 mg/1Tablet, CoatedOralRugby Laboratories0536-1292
AcetaminophenAcetaminophen 500 mg/1Tablet, Film coatedOralRugby Laboratories0536-1413
AcetaminophenAcetaminophen 325 mg/1Tablet, Film coatedOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8608
AcetaminophenAcetaminophen 325 mg/1Tablet, Film coatedOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8609

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