NDC codes

FDA NDC Directory
Product NDC (as listed)69842-635Labeler and product segments. Claims need a package NDC.
Product NDC at billing width69842-0635Add 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
69842-635-07698420635071 BOTTLE in 1 CARTON (69842-635-07) / 24 TABLET, EXTENDED RELEASE in 1 BOTTLEMarketed from Oct 13, 2022

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
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 207229
Marketing start
Listing expires
Identifiers
Product ID 69842-635_8394aaec-e897-48bb-bda2-cc2b64a6cd64SPL ID 8394aaec-e897-48bb-bda2-cc2b64a6cd64SPL set ID e577fdf0-85b1-1471-e053-2995a90a6fcdRxCUI 1148399UNII 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

N469842063507 followed by a unit qualifier and the quantity

Package 69842-0635-07. 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: muscular aches backache minor pain of arthritis toothache premenstrual and menstrual cramps headache the common cold temporarily reduces fever

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

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/1Tablet, Extended releaseOralWALGREEN CO.0363-9604
AcetaminophenAcetaminophen 650 mg/1TabletOralBluePoint Laboratories68001-495
Amazon Basic Care AcetaminophenacetaminophenAcetaminophen 650 mg/1Tablet, Extended releaseOralAmazon.com Services LLC72288-698
AcetaminophenAcetaminophen 650 mg/1Tablet, Extended releaseOralKROGER COMPANY30142-157
AcetaminophenAcetaminophen 650 mg/1TabletOralAmerican Health Packaging60687-924
AcetaminophenAcetaminophen 650 mg/1Tablet, Extended releaseOralAurohealth LLC58602-730
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 releaseOralWALMART INC.79903-132
AcetaminophenAcetaminophen 650 mg/1Tablet, Extended releaseOralAurohealth LLC58602-848
AcetaminophenAcetaminophen 650 mg/1Tablet, Extended releaseOralAurohealth LLC58602-873

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