Ibuprofen and Diphenhydramine HCl

Product NDC

68016-217

11-digit product format

680160217

Labeler code

68016

Product ID

68016-217_f36807e5-7af9-4164-aa19-f035abbe5a9c

Type

HUMAN OTC DRUG

Nonproprietary name

IBUPROFEN, DIPHENHYDRAMINE HCL

Dosage form

CAPSULE, LIQUID FILLED

Route

ORAL

Labeler

Chain Drug Consortium, LLC

Application

ANDA090397

Marketing category

ANDA

Marketing start

2013-01-04

Marketing end

2019-12-31

Substance

IBUPROFEN; DIPHENHYDRAMINE HYDROCHLORIDE

Active strength

200 mg/1; mg/1

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record