Hydrocortisone

Product NDC

50436-2144

11-digit product format

504362144

Labeler code

50436

Product ID

50436-2144_d1c3ba72-408f-4ef3-bd2d-c601dbedcfbd

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Hydrocortisone

Dosage form

CREAM

Route

TOPICAL

Labeler

Unit Dose Services

Application

ANDA088799

Marketing category

ANDA

Marketing start

2005-04-28

Marketing end

0000-00-00

Substance

HYDROCORTISONE

Active strength

25 mg/g

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record