HYDROCORTISONE

Product NDC
0904-7188
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
hydrocortisone
Dosage form
TABLET
Route
ORAL
Labeler
Major Pharmaceuticals
Application
ANDA040646
Marketing category
ANDA
Substance
HYDROCORTISONE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
0904-7188-61100 BLISTER PACK in 1 CARTON (0904-7188-61) / 1 TABLET in 1 BLISTER PACK2007-03-30NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Hydrocortisone Tablets, USP 5 mg, 10 mg and 20 mg Rx onlyMajor Pharmaceuticals2025-09-10HUMAN PRESCRIPTION DRUG LABEL3