Ibuprofen

Product NDC
41250-198
11-digit product format
412500198
Labeler code
41250
Product ID
41250-198_06311c14-061d-4a3f-b36d-f83cfa67d7d2
Type
HUMAN OTC DRUG
Nonproprietary name
Ibuprofen
Dosage form
CAPSULE, LIQUID FILLED
Route
ORAL
Labeler
MEIJER, INC.
Application
ANDA078682
Marketing category
ANDA
Marketing start
2010-07-12
Marketing end
2024-04-26
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
41250-198-16412500198162 BOTTLE, PLASTIC in 1 BOX (41250-198-16) > 80 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC2010-07-122024-04-26NoNoCurrent
41250-198-18412500198181 BOTTLE, PLASTIC in 1 BOX (41250-198-18) > 180 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC2010-07-122024-04-26NoNoCurrent
41250-198-3041250019830300 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (41250-198-30) 2010-07-122024-04-26NoNoCurrent
41250-198-40412500198401 BOTTLE, PLASTIC in 1 BOX (41250-198-40) > 40 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC2010-07-122024-04-26NoNoCurrent
41250-198-80412500198801 BOTTLE, PLASTIC in 1 BOX (41250-198-80) > 80 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC2010-07-122024-04-26NoNoCurrent