Ibuprofen PM

Product NDC

50844-732

11-digit product format

508440732

Labeler code

50844

Product ID

50844-732_2d143d62-b2a7-45d1-a671-17b0b95615f5

Type

HUMAN OTC DRUG

Nonproprietary name

Ibuprofen and Diphenhydramine HCl

Dosage form

CAPSULE, LIQUID FILLED

Route

ORAL

Labeler

LNK International, Inc.

Application

ANDA200888

Marketing category

ANDA

Marketing start

2012-03-05

Marketing end

0000-00-00

Substance

IBUPROFEN; DIPHENHYDRAMINE HYDROCHLORIDE

Active strength

200 mg/1; mg/1

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record