NDC 63824-072

Mucinex DM Maximum Strength

Guaifenesin And Dextromethorphan Hydrobromide

Mucinex DM Maximum Strength is a Oral Tablet, Extended Release in the Human Otc Drug category. It is labeled and distributed by Rb Health (us) Llc. The primary component is Guaifenesin; Dextromethorphan Hydrobromide.

Product ID63824-072_5cb19957-f25d-4280-b070-1a893095f8d4
NDC63824-072
Product TypeHuman Otc Drug
Proprietary NameMucinex DM Maximum Strength
Generic NameGuaifenesin And Dextromethorphan Hydrobromide
Dosage FormTablet, Extended Release
Route of AdministrationORAL
Marketing Start Date2012-06-26
Marketing CategoryNDA / NDA
Application NumberNDA021620
Labeler NameRB Health (US) LLC
Substance NameGUAIFENESIN; DEXTROMETHORPHAN HYDROBROMIDE
Active Ingredient Strength1200 mg/1; mg/1
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 63824-072-07

1 BLISTER PACK in 1 CARTON (63824-072-07) > 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Marketing Start Date2012-06-26
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 63824-072-48 [63824007248]

Mucinex DM Maximum Strength TABLET, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA021620
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2012-06-26

NDC 63824-072-36 [63824007236]

Mucinex DM Maximum Strength TABLET, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA021620
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2012-06-26

NDC 63824-072-35 [63824007235]

Mucinex DM Maximum Strength TABLET, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA021620
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2012-06-26

NDC 63824-072-46 [63824007246]

Mucinex DM Maximum Strength TABLET, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA021620
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2012-06-26

NDC 63824-072-71 [63824007271]

Mucinex DM Maximum Strength TABLET, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA021620
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-12-26
Marketing End Date2012-07-25

NDC 63824-072-45 [63824007245]

Mucinex DM Maximum Strength TABLET, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA021620
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2012-06-26
Marketing End Date2014-10-10

NDC 63824-072-07 [63824007207]

Mucinex DM Maximum Strength TABLET, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA021620
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2012-06-26

NDC 63824-072-39 [63824007239]

Mucinex DM Maximum Strength TABLET, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA021620
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-06-26
Marketing End Date2014-10-10

NDC 63824-072-18 [63824007218]

Mucinex DM Maximum Strength TABLET, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA021620
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-06-26

Drug Details

Active Ingredients

IngredientStrength
GUAIFENESIN1200 mg/1

OpenFDA Data

SPL SET ID:588eddc1-fa30-41cc-8ed9-c01319ea21c6
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1099074
  • 1298299

    • Medicade Reported Pricing

    63824072216 CEPACOL SORE THROAT LOZENGE

    Pricing Unit: EA | Drug Type:

    63824072016 CEPACOL SORE THROAT LOZENGE

    Pricing Unit: EA | Drug Type:

    63824007246 MUCINEX DM ER 1,200-60 MG TAB

    Pricing Unit: EA | Drug Type:

    63824007236 MUCINEX DM ER 1,200-60 MG TAB

    Pricing Unit: EA | Drug Type:

    63824007235 MUCINEX DM ER 1,200-60 MG TAB

    Pricing Unit: EA | Drug Type:

    NDC Crossover Matching brand name "Mucinex DM Maximum Strength" or generic name "Guaifenesin And Dextromethorphan Hydrobromide"

    NDCBrand NameGeneric Name
    63824-072Mucinex DM Maximum StrengthMucinex DM Maximum Strength
    0536-0970Extra action CoughGuaifenesin and DEXTROMETHORPHAN HYDROBROMIDE
    48433-221GUAIFENESIN AND DEXTROMETHORPHAN HBrguaifenesin and dextromethorphan hydrobromide
    0363-0076Guaifenesin and Dextromethorphan HydrobromideGuaifenesin and Dextromethorphan Hydrobromide
    11822-7156Guaifenesin and Dextromethorphan HydrobromideGuaifenesin and Dextromethorphan Hydrobromide
    24451-133Guaifenesin and Dextromethorphan HydrobromideGuaifenesin and Dextromethorphan Hydrobromide
    24689-123Guaifenesin and Dextromethorphan HydrobromideGuaifenesin and Dextromethorphan Hydrobromide
    30142-706Guaifenesin and Dextromethorphan HydrobromideGuaifenesin and Dextromethorphan Hydrobromide
    49035-077Guaifenesin and Dextromethorphan HydrobromideGuaifenesin and Dextromethorphan Hydrobromide
    11822-9996Guaifenesin and Dextromethorphan Hydrobromide HBRguaifenesin and dextromethorphan hydrobromide
    43063-801Guaifenesin DMGuaifenesin and Dextromethorphan Hydrobromide
    17856-0056Mucinex DMGuaifenesin and Dextromethorphan Hydrobromide
    50090-1077Mucinex DMGuaifenesin and Dextromethorphan Hydrobromide
    50090-1078Mucinex DMGuaifenesin and Dextromethorphan Hydrobromide
    50090-2298Mucinex DMGuaifenesin and Dextromethorphan Hydrobromide
    0363-9013MUCUS RELIEF DMGUAIFENESIN and DEXTROMETHORPHAN HYDROBROMIDE
    0363-9891MUCUS RELIEF DMGUAIFENESIN and DEXTROMETHORPHAN HYDROBROMIDE
    0363-9897MUCUS RELIEF DMGUAIFENESIN and DEXTROMETHORPHAN HYDROBROMIDE
    30142-991Mucus Relief ER DMGuaifenesin and Dextromethorphan Hydrobromide
    0904-0053Rabofen DMGuaifenesin and Dextromethorphan Hydrobromide
    0904-6306Robafen DM Cough Sugar Free ClearGuaifenesin and Dextromethorphan Hydrobromide
    17856-6306Robafen DM Cough Sugar Free ClearGuaifenesin and Dextromethorphan Hydrobromide
    17856-0134Siltussin DM DAS Cough FormulaGuaifenesin and Dextromethorphan Hydrobromide

    Trademark Results [Mucinex DM]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    MUCINEX DM
    MUCINEX DM
    88108705 5744739 Live/Registered
    RB HEALTH (US) LLC
    2018-09-07
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