Mucus Relief D

Product NDC

37808-446

11-digit product format

378080446

Labeler code

37808

Product ID

37808-446_b408c871-4f25-421a-8dd2-4770e4bedd00

Type

HUMAN OTC DRUG

Nonproprietary name

Guaifenesin, pseudoephedrine hydrochloride

Dosage form

TABLET, EXTENDED RELEASE

Route

ORAL

Labeler

H E B

Application

ANDA091071

Marketing category

ANDA

Marketing start

2016-03-22

Marketing end

0000-00-00

Substance

GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE

Active strength

600 mg/1; mg/1

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record