Ibuprofen

Product NDC
49035-121
11-digit product format
490350121
Labeler code
49035
Product ID
49035-121_fa79c1fa-e71c-447e-a24c-ab34834d7a99
Type
HUMAN OTC DRUG
Nonproprietary name
Ibuprofen
Dosage form
CAPSULE, LIQUID FILLED
Route
ORAL
Labeler
EQUATE (Wal-Mart Stores, Inc.)
Application
ANDA202300
Marketing category
ANDA
Marketing start
2015-02-28
Marketing end
2021-12-30
Substance
IBUPROFEN
Active strength
200 mg/1
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
49035-121-0349035012103300 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (49035-121-03) 2015-02-282021-12-30NoNoCurrent
49035-121-1649035012116160 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (49035-121-16) 2015-02-282021-12-30NoNoCurrent
49035-121-20490350121201 BOTTLE, PLASTIC in 1 BOX (49035-121-20) > 20 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC2015-02-282021-12-30NoNoCurrent
49035-121-40490350121401 BOTTLE, PLASTIC in 1 BOX (49035-121-40) > 40 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC2015-02-282021-12-30NoNoCurrent
49035-121-804903501218080 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (49035-121-80) 2015-02-282021-12-30NoNoCurrent