arthritis pain relief

Product NDC
30142-544
11-digit product format
301420544
Labeler code
30142
Product ID
30142-544_db35ea73-2fd9-47da-b480-9992b1f04672
Type
HUMAN OTC DRUG
Nonproprietary name
Acetaminophen
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
Kroger Company
Application
ANDA075077
Marketing category
ANDA
Marketing start
2000-06-06
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

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
30142-544-47301420544471 BOTTLE in 1 CARTON (30142-544-47) > 150 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE1 bottle2014-03-150000-00-00NoNoCurrent
30142-544-62301420544621 BOTTLE in 1 CARTON (30142-544-62) > 24 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE1 bottle2018-06-010000-00-00NoNoCurrent
30142-544-71301420544711 BOTTLE in 1 CARTON (30142-544-71) > 50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE1 bottle2000-06-130000-00-00NoNoCurrent
30142-544-76301420544761 BOTTLE in 1 CARTON (30142-544-76) > 120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE1 bottle2016-08-090000-00-00NoNoCurrent
30142-544-78301420544781 BOTTLE in 1 CARTON (30142-544-78) > 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE1 bottle2000-06-060000-00-00NoNoCurrent
30142-544-8530142054485250 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (30142-544-85) 2013-04-210000-00-00NoNoCurrent