Ibuprofen PM

Product NDC

50804-165

11-digit product format

508040165

Labeler code

50804

Product ID

50804-165_a04a4e04-5507-4b2e-84a2-ec644eb23d0c

Type

HUMAN OTC DRUG

Nonproprietary name

Ibuprofen and Diphenhydramine HCl

Dosage form

CAPSULE, LIQUID FILLED

Route

ORAL

Labeler

Good Sense (Geiss, Destin & Dunn, Inc.)

Application

ANDA090397

Marketing category

ANDA

Marketing start

2013-01-15

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