BETAMETHASONE DIPROPIONATE

Product NDC
72162-1415
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
betamethasone dipropionate
Dosage form
OINTMENT
Route
TOPICAL
Labeler
Bryant Ranch Prepack
Application
ANDA215847
Marketing category
ANDA
Substance
BETAMETHASONE DIPROPIONATE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
72162-1415-21 TUBE in 1 CARTON (72162-1415-2) / 45 g in 1 TUBE2024-03-12NoHistorical
72162-1415-41 TUBE in 1 CARTON (72162-1415-4) / 15 g in 1 TUBE2024-03-12NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
BETAMETHASONE DIPROPIONATE OINTMENT USP, 0.05%Bryant Ranch Prepack2025-09-12HUMAN PRESCRIPTION DRUG LABEL101