Ibuprofen

Product NDC
0472-1764
11-digit product format
004721764
Labeler code
0472
Product ID
0472-1764_6558b400-0340-46c2-9825-4001acd48528
Type
HUMAN OTC DRUG
Nonproprietary name
Ibuprofen
Dosage form
SUSPENSION
Route
ORAL
Labeler
Actavis Pharma, Inc.
Application
ANDA074916
Marketing category
ANDA
Marketing start
2016-09-13
Marketing end
2022-10-31
Substance
IBUPROFEN
Active strength
100 mg/5mL
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0472-1764-94ML - Milliliter0472-1764d0196656-dc46-4d0e-940d-534548a9dcc412016-09-02

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0472-1764-94004721764941 BOTTLE in 1 CARTON (0472-1764-94) > 118 mL in 1 BOTTLE1 bottle2016-09-130000-00-00NoNoCurrent