Budesonide

Product NDC

60687-421

11-digit product format

606870421

Labeler code

60687

Product ID

60687-421_890595a4-5a83-7af9-e053-2a95a90a2a5c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

budesonide

Dosage form

CAPSULE

Route

ORAL

Labeler

American Health Packaging

Application

ANDA207367

Marketing category

ANDA

Marketing start

2018-12-18

Marketing end

2020-05-31

Substance

BUDESONIDE

Active strength

3 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