Ibuprofen

Product NDC
72036-111
11-digit product format
720360111
Labeler code
72036
Product ID
72036-111_94980ed7-d37d-de9f-e053-2a95a90aa81f
Type
HUMAN OTC DRUG
Nonproprietary name
Ibuprofen
Dosage form
TABLET, COATED
Route
ORAL
Labeler
Harris Teeter
Application
ANDA091355
Marketing category
ANDA
Marketing start
2012-09-18
Marketing end
0000-00-00
Substance
IBUPROFEN
Active strength
200 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 formatDescriptionMarketing startMarketing endSampleExclude flagStatus
72036-111-02720360111021 BOTTLE, PLASTIC in 1 CARTON (72036-111-02) > 50 TABLET, COATED in 1 BOTTLE, PLASTIC2012-09-180000-00-00NoNoCurrent
72036-111-03720360111031 BOTTLE, PLASTIC in 1 CARTON (72036-111-03) > 100 TABLET, COATED in 1 BOTTLE, PLASTIC2012-09-180000-00-00NoNoCurrent