NDC 58605-101

Maxifed

Guaifenesin And Pseudoephedrine Hydrochloride

Maxifed is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Mcr American Pharmaceuticals, Inc.. The primary component is Guaifenesin; Pseudoephedrine Hydrochloride.

Product ID58605-101_f954e296-1429-4985-9d04-a20b67e2cf71
NDC58605-101
Product TypeHuman Otc Drug
Proprietary NameMaxifed
Generic NameGuaifenesin And Pseudoephedrine Hydrochloride
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2018-04-01
Marketing CategoryOTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
Application Numberpart341
Labeler NameMCR American Pharmaceuticals, Inc.
Substance NameGUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE
Active Ingredient Strength360 mg/1; mg/1
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 58605-101-01

100 TABLET in 1 BOTTLE, PLASTIC (58605-101-01)
Marketing Start Date2018-04-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 58605-101-20 [58605010120]

Maxifed TABLET
Marketing CategoryOTC monograph final
Application Numberpart341
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-04-01

NDC 58605-101-01 [58605010101]

Maxifed TABLET
Marketing CategoryOTC monograph final
Application Numberpart341
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2018-04-01

Drug Details

Active Ingredients

IngredientStrength
GUAIFENESIN360 mg/1

OpenFDA Data

SPL SET ID:8a1be614-2a78-4899-9697-774479f2daa5
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 2003123

    • NDC Crossover Matching brand name "Maxifed" or generic name "Guaifenesin And Pseudoephedrine Hydrochloride"

    NDCBrand NameGeneric Name
    58605-101MaxifedGUAIFENESIN and Pseudoephedrine Hydrochloride
    66992-281Entex TGuaifenesin and Pseudoephedrine Hydrochloride
    79903-125equate mucus dguaifenesin and pseudoephedrine hydrochloride
    0363-0077Guaifenesin and Pseudoephedrine HydrochlorideGuaifenesin and Pseudoephedrine Hydrochloride
    41415-994Guaifenesin and Pseudoephedrine HydrochlorideGuaifenesin and Pseudoephedrine Hydrochloride
    51660-071Guaifenesin and Pseudoephedrine HydrochlorideGuaifenesin and Pseudoephedrine Hydrochloride
    62011-0475Guaifenesin and Pseudoephedrine HydrochlorideGuaifenesin and Pseudoephedrine Hydrochloride
    0363-9930Guaifenesin DGuaifenesin and Pseudoephedrine Hydrochloride
    0536-1333Guaifenesin DGuaifenesin and Pseudoephedrine Hydrochloride
    51316-993Guaifenesin DGuaifenesin and Pseudoephedrine Hydrochloride
    70000-0580Guaifenesin DGuaifenesin and Pseudoephedrine Hydrochloride
    51316-970MAXIMUM STRENGTH Mucus Dguaifenesin and pseudoephedrine hydrochloride
    50090-1075Mucinex DGuaifenesin and Pseudoephedrine Hydrochloride
    50090-1076Mucinex DGuaifenesin and Pseudoephedrine Hydrochloride
    63824-041Mucinex DGuaifenesin and Pseudoephedrine Hydrochloride
    63824-057Mucinex DGuaifenesin and Pseudoephedrine Hydrochloride
    68258-3035Mucinex DGuaifenesin and Pseudoephedrine Hydrochloride
    70518-0523Mucinex DGuaifenesin and Pseudoephedrine Hydrochloride
    0536-1137Mucus Relief DGuaifenesin and Pseudoephedrine Hydrochloride

    Trademark Results [Maxifed]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    MAXIFED
    MAXIFED
    75130397 2242345 Live/Registered
    MCR American Pharmaceuticals, Inc.
    1996-07-05
    MAXIFED
    MAXIFED
    74546782 not registered Dead/Abandoned
    JOHNSON & JOHNSON
    1994-07-07
    MAXIFED
    MAXIFED
    74026406 not registered Dead/Abandoned
    Johnson & Johnson
    1990-02-06
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