Dexamethasone

Product NDC
72789-501
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Dexamethasone
Dosage form
TABLET
Route
ORAL
Labeler
PD-Rx Pharmaceuticals, Inc.
Application
ANDA216282
Marketing category
ANDA
Substance
DEXAMETHASONE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
72789-501-2020 TABLET in 1 BOTTLE, PLASTIC (72789-501-20) 2025-04-30NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Dexamethasone Tablets, USPPD-Rx Pharmaceuticals, Inc.2025-04-30HUMAN PRESCRIPTION DRUG LABEL2