good sense ibuprofen

Product NDC
68788-4051
11-digit product format
687884051
Labeler code
68788
Product ID
68788-4051_c447fc6b-e9ef-447a-9609-5f893e18dfa7
Type
HUMAN OTC DRUG
Nonproprietary name
Ibuprofen
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Preferred Pharmaceuticals Inc.
Application
ANDA072096
Marketing category
ANDA
Marketing start
2025-11-17
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
2026-12-31
Current FDA listing
Yes

Additional Listing Data

Finished product
Yes
Brand name base
good sense ibuprofen
Listing expiration
2026-12-31

Related Records

Active Ingredients

IngredientStrength
IBUPROFEN200 mg/1

Harmonized Identifiers

FieldValues
UniiWK2XYI10QM
Rxcui310965

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
WK2XYI10QMIBUPROFEN15687-27-1IBUPROFEN

Packages

Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
68788-4051-168788405101100 TABLET, FILM COATED in 1 BOTTLE (68788-4051-1) 2025-11-17NoNoCurrent
68788-4051-36878840510330 TABLET, FILM COATED in 1 BOTTLE (68788-4051-3) 2025-11-17NoNoCurrent
68788-4051-56878840510550 TABLET, FILM COATED in 1 BOTTLE (68788-4051-5) 2025-11-17NoNoCurrent

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Perrigo Ibuprofen Tablets, 200 mg Drug FactsPreferred Pharmaceuticals Inc.2025-11-17HUMAN OTC DRUG LABEL1