Ibuprofen

Product NDC
68391-199
11-digit product format
683910199
Labeler code
68391
Product ID
68391-199_c8eba165-67d4-497a-98dd-42b4b17592dd
Type
HUMAN OTC DRUG
Nonproprietary name
Ibuprofen
Dosage form
CAPSULE, LIQUID FILLED
Route
ORAL
Labeler
BJWC (Berkley & Jensen / BJ's)
Application
ANDA078682
Marketing category
ANDA
Marketing start
2013-05-15
Marketing end
2024-05-15
Substance
IBUPROFEN
Active strength
200 mg/1
Pharmacologic classes
Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
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 formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68391-199-24683910199241 BOTTLE in 1 BOX (68391-199-24) > 240 CAPSULE, LIQUID FILLED in 1 BOTTLE1 bottle2013-05-150000-00-00NoNoCurrent