Childrens RHINOCORT Allergy

Product NDC

50580-510

11-digit product format

505800510

Labeler code

50580

Product ID

50580-510_96c65ef7-bc67-4b65-b365-3a46f1805b7b

Type

HUMAN OTC DRUG

Nonproprietary name

Budesonide

Dosage form

SPRAY, METERED

Route

NASAL

Labeler

Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division

Application

NDA020746

Marketing category

NDA

Marketing start

2017-01-16

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