Acetaminophen

Product NDC
46122-170
11-digit product format
461220170
Labeler code
46122
Product ID
46122-170_c7cc85d7-e528-4cdc-8550-7e431c10c3a5
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
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
46122-170-81EA - Each46122-1707eb41e27-2d7f-4a61-ae5c-a45b112d407e12013-02-13

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
46122-170ACETAMINOPHEN TABLET, FILM COATED, EXTENDED RELEASE [AMERISOURCE BERGEN]2Legacy NDC20190411_71be6a5b-aff2-4757-804a-085b44e2a7d3.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
46122-170-8146122017081200 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46122-170-81) 2002-04-300000-00-00NoNoCurrent