NDC codes

FDA NDC Directory
Product NDC (as listed)63941-456Labeler and product segments. Claims need a package NDC.
Product NDC at billing width63941-0456Add 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
63941-456-02639410456021 BOTTLE, PLASTIC in 1 CARTON (63941-456-02) / 100 TABLET in 1 BOTTLE, PLASTICMarketed from Feb 5, 2010

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)
Regular Strength Pain Relief
Generic name (nonproprietary)
acetaminophen
Active ingredients
Acetaminophen — 325 mg/1
Dosage form
Tablet
Route
Oral
Labeler
VALU MERCHANDISERS COMPANYNDC labeler code 63941
Product type
Over-the-counter drug
Marketing category
OTC monograph drugApplication M 013
Marketing start
Marketing end
Identifiers
Product ID 63941-456_45b2f5cd-326d-053a-e063-6294a90ab685SPL ID 45b2f5cd-326d-053a-e063-6294a90ab685SPL set ID f7e87eac-59fb-4a72-b5c6-02953112be6aRxCUI 313782UNII 362O9ITL9DUPC 0070038201717

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

N463941045602 followed by a unit qualifier and the quantity

Package 63941-0456-02. 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 .

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 63941-456

What is NDC 63941-456?
63941-456 is the product NDC for Regular Strength Pain Relief (acetaminophen), Acetaminophen 325 mg/1 tablet, listed with the FDA by VALU MERCHANDISERS COMPANY. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Regular Strength Pain Relief (Acetaminophen).
What is the active ingredient?
Acetaminophen.
Who is the labeler?
VALU MERCHANDISERS COMPANY, NDC labeler code 63941. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Regular Strength Pain Relief?
5 other product NDCs are listed under this name. See all Regular Strength Pain Relief 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 Regular Strength Pain Relief NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Regular Strength Pain ReliefacetaminophenAcetaminophen 325 mg/1Capsule, Liquid filledOralBelmora LLC27854-38827854-0388-01
Regular Strength Pain ReliefacetaminophenAcetaminophen 325 mg/1TabletOralGeri-Care Pharmaceutical Corp57896-10257896-0102-0157896-0102-0557896-0102-10+1 more
Regular Strength Pain ReliefacetaminophenAcetaminophen 325 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-356568071-3565-00
Regular Strength Pain ReliefacetaminophenAcetaminophen 325 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-465668071-4656-05
Regular Strength Pain ReliefacetaminophenAcetaminophen 325 mg/1TabletOralBryant Ranch Prepack72162-225272162-2252-01

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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