Hydrocortisone

Product NDC

0603-3901

11-digit product format

006033901

Labeler code

0603

Product ID

0603-3901_922778c7-7e86-4fe8-8a5b-5e4d0ad066ab

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

hydrocortisone

Dosage form

TABLET

Route

ORAL

Labeler

Par Pharmaceutical

Application

ANDA040761

Marketing category

ANDA

Marketing start

2007-07-16

Marketing end

2019-09-30

Substance

HYDROCORTISONE

Active strength

20 mg/1

Pharmacologic classes

Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record