Acetaminophen

Product NDC
46122-062
11-digit product format
461220062
Labeler code
46122
Product ID
46122-062_d0ea1815-1f04-4c23-9761-307116c04b63
Type
HUMAN OTC DRUG
Nonproprietary name
Acetaminophen
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
Amerisource Bergen
Application
ANDA076200
Marketing category
ANDA
Marketing start
2002-04-30
Marketing end
0000-00-00
Substance
ACETAMINOPHEN
Active strength
650 mg/1
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
46122-062-71EA - Each46122-062b57b5b58-642c-445b-b917-44a594a9d2c312013-02-13
46122-062-78EA - Each46122-0624d0e3d35-74fc-4895-9da8-b2ab29aa912312013-02-13

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
46122-062ACETAMINOPHEN TABLET, FILM COATED, EXTENDED RELEASE [AMERISOURCE BERGEN]7Legacy NDC20250119_c0f4d7f1-aa17-4233-bc47-41c280fdd7ce.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
46122-062-714612200627150 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46122-062-71) 2002-04-300000-00-00NoNoCurrent
46122-062-7846122006278100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46122-062-78) 2002-04-300000-00-00NoNoCurrent