Ibuprofen

Product NDC
0472-1760
11-digit product format
004721760
Labeler code
0472
Product ID
0472-1760_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
2018-01-12
Marketing end
0000-00-00
Substance
IBUPROFEN
Active strength
100 mg/5mL
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0472-1760-94ML - Milliliter0472-1760fa1efcc4-e467-46d9-8969-9e6602f2d1ed12018-03-08
0472-1760-98ML - Milliliter0472-1760b39d8cbc-3af1-4fb9-9f95-9d9d45c1790912018-02-20

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0472-1760-94004721760941 BOTTLE in 1 CARTON (0472-1760-94) > 118 mL in 1 BOTTLE1 bottle2018-02-210000-00-00NoNoCurrent
0472-1760-98004721760981 BOTTLE in 1 CARTON (0472-1760-98) > 237 mL in 1 BOTTLE1 bottle2018-01-120000-00-00NoNoCurrent