rx act ibuprofen pm

Product NDC

37808-050

11-digit product format

378080050

Labeler code

37808

Product ID

37808-050_51d69fcf-3d70-485c-ab77-a10bf2e0af78

Type

HUMAN OTC DRUG

Nonproprietary name

diphenhydramine citrate, ibuprofen

Dosage form

TABLET, COATED

Route

ORAL

Labeler

H E B

Application

ANDA079113

Marketing category

ANDA

Marketing start

2009-03-11

Marketing end

0000-00-00

Substance

DIPHENHYDRAMINE CITRATE; IBUPROFEN

Active strength

38 mg/1; mg/1

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record