7 Select Ibuprofen PM

Product NDC

10202-050

11-digit product format

102020050

Labeler code

10202

Product ID

10202-050_8fd58a88-b0d6-4b8d-a993-5ce187dca8a5

Type

HUMAN OTC DRUG

Nonproprietary name

diphenhydramine citrate, ibuprofen

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

7-Eleven

Application

ANDA079113

Marketing category

ANDA

Marketing start

2014-08-05

Marketing end

2020-11-30

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