Desonide

Product NDC
46708-632
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Desonide
Dosage form
CREAM
Route
TOPICAL
Labeler
Alembic Pharmaceuticals Limited
Application
ANDA214396
Marketing category
ANDA
Substance
DESONIDE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
46708-632-151 TUBE in 1 CARTON (46708-632-15) / 15 g in 1 TUBE2025-04-29NoHistorical
46708-632-601 TUBE in 1 CARTON (46708-632-60) / 60 g in 1 TUBE2025-04-29NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Desonide Cream, 0.05% For Dermatologic Use Only Not For Ophthalmic Use Rx OnlyAlembic Pharmaceuticals Limited2025-04-11HUMAN PRESCRIPTION DRUG LABEL1