Budesonide

Product NDC

11822-6000

11-digit product format

118226000

Labeler code

11822

Product ID

11822-6000_4b3e3509-2c5a-f44c-8dce-5f767f3a9a3c

Type

HUMAN OTC DRUG

Nonproprietary name

Budesonide

Dosage form

SPRAY, METERED

Route

NASAL

Labeler

Rite Aid

Application

ANDA078949

Marketing category

ANDA

Marketing start

2016-07-13

Marketing end

0000-00-00

Substance

BUDESONIDE

Active strength

32 ug/1

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record