Ibuprofen

Product NDC
61715-061
11-digit product format
617150061
Labeler code
61715
Product ID
61715-061_c1b1f1ae-db9d-4326-996b-af018abb687b
Type
HUMAN OTC DRUG
Nonproprietary name
Ibuprofen
Dosage form
TABLET
Route
ORAL
Labeler
Kinray
Application
ANDA091239
Marketing category
ANDA
Marketing start
2011-07-25
Marketing end
0000-00-00
Substance
IBUPROFEN
Active strength
200 mg/1
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
61715-061-512025-05-22C16284748780-19d75b9d1-1821-f424-e053-dadaa90a57cea74cfe5d-0249-4925-83d3-e8bb233ec05c
61715-061-512020-01-31C16284748780-19d75b9d1-1821-f424-e053-dadaa90a57cea74cfe5d-0249-4925-83d3-e8bb233ec05c