Maxi-Tuss DM

Product NDC

58605-304

11-digit product format

586050304

Labeler code

58605

Product ID

58605-304_802aca7b-6aea-4829-ab9b-bc83a03f6f78

Type

HUMAN OTC DRUG

Nonproprietary name

CHLORPHENIRAMINE MALEATE and Dextromethorphan Hydrobromide

Dosage form

LIQUID

Route

ORAL

Labeler

MCR American Pharmaceuticals, Inc.

Application

part341

Marketing category

OTC MONOGRAPH FINAL

Marketing start

2018-04-01

Marketing end

0000-00-00

Substance

CHLORPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE

Active strength

4 mg/5mL; mg/5mL

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record