Sunmark ibuprofen

Product NDC
49348-876
11-digit product format
493480876
Labeler code
49348
Product ID
49348-876_baf2f7f9-5c99-414e-89b3-60bb4f1bf63d
Type
HUMAN OTC DRUG
Nonproprietary name
Ibuprofen
Dosage form
SUSPENSION
Route
ORAL
Labeler
Strategic Sourcing Services LLC
Application
ANDA074937
Marketing category
ANDA
Marketing start
2009-04-01
Marketing end
0000-00-00
Substance
IBUPROFEN
Active strength
100 mg/5mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
49348-876-34ML - Milliliter49348-876c7124475-9a76-4d08-803d-5e116e4e980912012-07-24

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
49348-876-34493480876341 BOTTLE in 1 CARTON (49348-876-34) > 120 mL in 1 BOTTLE1 bottle2009-04-010000-00-00NoNoCurrent