NDC codes

FDA NDC Directory
Product NDC (as listed)30142-157Labeler and product segments. Claims need a package NDC.
Product NDC at billing width30142-0157Add 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
30142-157-0730142015707301420157071 BOTTLE in 1 CARTON (30142-157-07) / 24 TABLET, EXTENDED RELEASE in 1 BOTTLEMarketed from May 25, 2021
30142-157-353014201573530142015735225 TABLET, EXTENDED RELEASE in 1 BOTTLE (30142-157-35)Marketed from May 25, 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, Extended release
Route
Oral
Labeler
KROGER COMPANYNDC labeler code 30142
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 207229
Marketing start
Listing expires
Identifiers
Product ID 30142-157_5cd5f635-7f27-4b34-bb0b-779d36c25398SPL ID 5cd5f635-7f27-4b34-bb0b-779d36c25398SPL set ID b9b63c38-83e7-62d2-e053-2a95a90a5526RxCUI 1148399UNII 362O9ITL9DUPC 0041260016325

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

N430142015707 followed by a unit qualifier and the quantity

Package 30142-0157-07. 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: 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 30142-157

What is NDC 30142-157?
30142-157 is the product NDC for Acetaminophen, Acetaminophen 650 mg/1 tablet, extended release, listed with the FDA by KROGER COMPANY. 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?
KROGER COMPANY, NDC labeler code 30142. 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
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
acetaminophenAcetaminophen 500 mg/1TabletOralREMEDYREPACK INC.70518-478770518-4787-00
AcetaminophenAcetaminophen 325 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-478270518-4782-0070518-4782-01
AcetaminophenAcetaminophen 500 mg/1TabletOralREMEDYREPACK INC.70518-478370518-4783-00
AcetaminophenAcetaminophen 500 mg/1TabletOralAmazon.com Services LLC72288-44072288-0440-09
acetaminophenAcetaminophen 650 mg/1Tablet, Film coated, Extended releaseOralAmazon.com Services LLC72288-15072288-0150-79
AcetaminophenAcetaminophen 10 mg/mLInjection, SolutionIntravenousSomerset Therapeutics, LLC70069-87170069-0871-10
AcetaminophenAcetaminophen 500 mg/1TabletOralWalgreens0363-981000363-9810-1000363-9810-2500363-9810-50+1 more
AcetaminophenAcetaminophen 500 mg/1TabletOralPUBLIX SUPERMARKETS, INC41415-17541415-0175-0541415-0175-10
AcetaminophenAcetaminophen 500 mg/1TabletOralFamily Dollar, Inc.55319-75155319-0751-24
AcetaminophenAcetaminophen 500 mg/1TabletOralMeijer Distribution Inc79481-078079481-0780-0179481-0780-0279481-0780-04

All 235 Acetaminophen NDCs

Other NDCs under ANDA 207229

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

FDA NDC Directory listings under ANDA 207229
ProductStrengthForm · routeLabelerProduct NDC
AcetaminophenAcetaminophen 650 mg/1TabletOralBluePoint Laboratories68001-495
AcetaminophenAcetaminophen 650 mg/1TabletOralAmerican Health Packaging60687-924
AcetaminophenAcetaminophen 650 mg/1Tablet, Extended releaseOralAurohealth LLC58602-730
AcetaminophenAcetaminophen 650 mg/1Tablet, Extended releaseOralWALGREEN CO.0363-9604
AcetaminophenAcetaminophen 650 mg/1Tablet, Extended releaseOralBetter Living Brands, LLC21130-108
AcetaminophenAcetaminophen 650 mg/1Tablet, Extended releaseOralCVS Pharmacy, Inc.69842-037
AcetaminophenAcetaminophen 650 mg/1Tablet, Extended releaseOralCVS Pharmacy, Inc.69842-635
Amazon Basic Care AcetaminophenacetaminophenAcetaminophen 650 mg/1Tablet, Extended releaseOralAmazon.com Services LLC72288-698
AcetaminophenAcetaminophen 650 mg/1Tablet, Extended releaseOralWALMART INC.79903-132
AcetaminophenAcetaminophen 650 mg/1Tablet, Extended releaseOralAurohealth LLC58602-848
AcetaminophenAcetaminophen 650 mg/1Tablet, Extended releaseOralAurohealth LLC58602-873

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