Ibuprofen

Product NDC
30142-198
11-digit product format
301420198
Labeler code
30142
Product ID
30142-198_aa31444b-5c7f-4725-8caf-76837b02efc8
Type
HUMAN OTC DRUG
Nonproprietary name
IBUPROFEN
Dosage form
CAPSULE, LIQUID FILLED
Route
ORAL
Labeler
The Kroger Co.
Application
ANDA078682
Marketing category
ANDA
Marketing start
2010-07-01
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
30142-198-0330142019803300 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (30142-198-03) 2010-07-012021-12-30NoNoCurrent
30142-198-1630142019816160 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (30142-198-16) 2010-07-012021-12-30NoNoCurrent
30142-198-20301420198201 BOTTLE, PLASTIC in 1 BOX (30142-198-20) > 20 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC2010-07-012021-12-30NoNoCurrent
30142-198-40301420198401 BOTTLE, PLASTIC in 1 BOX (30142-198-40) > 40 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC2010-07-012021-12-30NoNoCurrent
30142-198-803014201988080 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (30142-198-80) 2010-07-012021-12-30NoNoCurrent