Leader ibuprofen pm

Product NDC

37205-360

11-digit product format

372050360

Labeler code

37205

Product ID

37205-360_caed4f5d-9b7d-464f-a71d-6580d49773a0

Type

HUMAN OTC DRUG

Nonproprietary name

diphenhydramine citrate, ibuprofen

Dosage form

TABLET, COATED

Route

ORAL

Labeler

Cardinal Health

Application

ANDA079113

Marketing category

ANDA

Marketing start

2009-04-27

Marketing end

2019-09-30

Substance

DIPHENHYDRAMINE CITRATE; IBUPROFEN

Active strength

38 mg/1; mg/1

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record