Ibuprofen

Product NDC
21130-749
11-digit product format
211300749
Labeler code
21130
Product ID
21130-749_d34c5940-4f6f-4c7d-9556-97cdc46bdeee
Type
HUMAN OTC DRUG
Nonproprietary name
Ibuprofen
Dosage form
CAPSULE, LIQUID FILLED
Route
ORAL
Labeler
Safeway, Inc.
Application
ANDA206999
Marketing category
ANDA
Marketing start
2018-09-30
Marketing end
2022-12-30
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
21130-749-0321130074903300 CAPSULE, LIQUID FILLED in 1 BOTTLE (21130-749-03) 2018-09-302022-12-30NoNoCurrent
21130-749-1821130074918180 CAPSULE, LIQUID FILLED in 1 BOTTLE (21130-749-18) 2018-09-302022-12-30NoNoCurrent
21130-749-20211300749201 BOTTLE, PLASTIC in 1 BOX (21130-749-20) > 20 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC2018-09-302022-12-30NoNoCurrent
21130-749-40211300749401 BOTTLE, PLASTIC in 1 BOX (21130-749-40) > 40 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC2018-09-302022-12-30NoNoCurrent
21130-749-80211300749801 BOTTLE, PLASTIC in 1 BOX (21130-749-80) > 80 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC2018-09-302022-12-30NoNoCurrent