Ibuprofen

Product NDC
30142-750
11-digit product format
301420750
Labeler code
30142
Product ID
30142-750_01cc030f-6b09-4fcf-8c39-0d1aa55b6c35
Type
HUMAN OTC DRUG
Nonproprietary name
Ibuprofen
Dosage form
CAPSULE, LIQUID FILLED
Route
ORAL
Labeler
The Kroger Co.
Application
ANDA206999
Marketing category
ANDA
Marketing start
2018-08-31
Marketing end
2024-05-31
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
30142-750-0230142075002200 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (30142-750-02) 2018-08-312024-05-31NoNoCurrent
30142-750-1630142075016160 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (30142-750-16) 2018-08-312024-05-31NoNoCurrent
30142-750-20301420750201 BOTTLE, PLASTIC in 1 BOX (30142-750-20) > 20 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC2018-08-312024-05-31NoNoCurrent
30142-750-40301420750401 BOTTLE, PLASTIC in 1 BOX (30142-750-40) > 40 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC2018-08-312024-05-31NoNoCurrent
30142-750-803014207508080 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (30142-750-80) 2018-08-312024-05-31NoNoCurrent