NDC 63824-008

Mucinex

Guaifenesin

Mucinex 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.

Product ID63824-008_2d9afa3b-750d-45a7-aa97-b8290319dffd
NDC63824-008
Product TypeHuman Otc Drug
Proprietary NameMucinex
Generic NameGuaifenesin
Dosage FormTablet, Extended Release
Route of AdministrationORAL
Marketing Start Date2012-07-03
Marketing CategoryNDA / NDA
Application NumberNDA021282
Labeler NameRB Health (US) LLC
Substance NameGUAIFENESIN
Active Ingredient Strength600 mg/1
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 63824-008-15

5 BLISTER PACK in 1 CARTON (63824-008-15) > 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Marketing Start Date2012-07-03
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 63824-008-32 [63824000832]

Mucinex TABLET, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA021282
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2012-07-03

NDC 63824-008-72 [63824000872]

Mucinex TABLET, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA021282
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-07-03

NDC 63824-008-27 [63824000827]

Mucinex TABLET, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA021282
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2012-07-03

NDC 63824-008-86 [63824000886]

Mucinex TABLET, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA021282
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2012-07-03

NDC 63824-008-12 [63824000812]

Mucinex TABLET, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA021282
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-06-16
Marketing End Date2014-09-12

NDC 63824-008-74 [63824000874]

Mucinex TABLET, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA021282
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-07-03

NDC 63824-008-15 [63824000815]

Mucinex TABLET, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA021282
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2012-07-03

NDC 63824-008-17 [63824000817]

Mucinex TABLET, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA021282
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-10-01

NDC 63824-008-34 [63824000834]

Mucinex TABLET, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA021282
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2012-07-03

NDC 63824-008-10 [63824000810]

Mucinex TABLET, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA021282
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2012-07-03
Marketing End Date2014-09-12

NDC 63824-008-80 [63824000880]

Mucinex TABLET, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA021282
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-07-03

NDC 63824-008-62 [63824000862]

Mucinex TABLET, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA021282
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2011-06-16
Marketing End Date2014-09-12

NDC 63824-008-69 [63824000869]

Mucinex TABLET, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA021282
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2012-07-03

NDC 63824-008-24 [63824000824]

Mucinex TABLET, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA021282
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-07-03

NDC 63824-008-36 [63824000836]

Mucinex TABLET, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA021282
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2012-07-03

NDC 63824-008-73 [63824000873]

Mucinex TABLET, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA021282
Product TypeHUMAN OTC DRUG
Marketing Start Date2014-09-12

NDC 63824-008-92 [63824000892]

Mucinex TABLET, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA021282
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-07-03

NDC 63824-008-50 [63824000850]

Mucinex TABLET, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA021282
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2012-07-03

NDC 63824-008-61 [63824000861]

Mucinex TABLET, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA021282
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2012-07-03
Marketing End Date2014-09-12

Drug Details

Active Ingredients

IngredientStrength
GUAIFENESIN600 mg/1

OpenFDA Data

SPL SET ID:dd379cdd-90ab-42e0-ad89-f50d3220f611
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 636522
  • 891301
    • UPC Code
  • 0363824008202

    • Medicade Reported Pricing

    63824000886 MUCINEX ER 600 MG TABLET

    Pricing Unit: EA | Drug Type:

    63824000869 MUCINEX ER 600 MG TABLET

    Pricing Unit: EA | Drug Type:

    63824000861 MUCINEX ER 600 MG TABLET

    Pricing Unit: EA | Drug Type:

    63824000850 MUCINEX ER 600 MG TABLET

    Pricing Unit: EA | Drug Type:

    63824000840 MUCINEX ER 600 MG TABLET

    Pricing Unit: EA | Drug Type:

    63824000836 MUCINEX ER 600 MG TABLET

    Pricing Unit: EA | Drug Type:

    63824000834 MUCINEX ER 600 MG TABLET

    Pricing Unit: EA | Drug Type:

    63824000832 MUCINEX ER 600 MG TABLET

    Pricing Unit: EA | Drug Type:

    63824000827 MUCINEX ER 600 MG TABLET

    Pricing Unit: EA | Drug Type:

    63824000820 MUCINEX ER 600 MG TABLET

    Pricing Unit: EA | Drug Type:

    63824000815 MUCINEX ER 600 MG TABLET

    Pricing Unit: EA | Drug Type:

    63824000810 MUCINEX ER 600 MG TABLET

    Pricing Unit: EA | Drug Type:

    NDC Crossover Matching brand name "Mucinex" or generic name "Guaifenesin"

    NDCBrand NameGeneric Name
    68084-572MucinexMucinex
    70518-0228MucinexMucinex
    70518-0466MucinexMucinex
    17856-0008MucinexMucinex
    21695-870MucinexMucinex
    50090-0818MucinexMucinex
    50090-1340MucinexMucinex
    50090-2380MucinexMucinex
    53808-0871MucinexMucinex
    55045-3143MUCINEXMUCINEX
    55154-4680MucinexMucinex
    55700-489MucinexMucinex
    61919-651MUCINEXMUCINEX
    63187-954MucinexMucinex
    63629-7115MucinexMucinex
    63629-7886MucinexMucinex
    63824-008MucinexMucinex
    67544-149MucinexMucinex
    0363-0288childrens chest congestionGuaifenesin
    0113-0325Good Sense Mucus ERGuaifenesin
    0113-2023good sense mucus erguaifenesin
    0113-3650Good Sense Mucus ERGuaifenesin
    0113-0061good sense tussinGuaifenesin
    0121-0744GUAIFENESINGUAIFENESIN
    0121-1488GUAIFENESINGUAIFENESIN
    0121-1744GUAIFENESINGUAIFENESIN
    0121-2232GUAIFENESINGUAIFENESIN
    0363-0028GuaifenesinGuaifenesin
    0363-0033GuaifenesinGuaifenesin
    0363-0071MucusGuaifenesin
    0363-0074MucusGuaifenesin
    0363-0532Mucus ReliefGuaifenesin
    0363-0325mucus relief erGuaifenesin
    0031-9303Robitussin Direct Chest Congestionguaifenesin
    0031-8724Robitussin Mucus Plus Chest CongestionGuaifenesin
    0113-2061tussinGuaifenesin
    0363-0310wal tussinGuaifenesin

    Trademark Results [Mucinex]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    MUCINEX
    MUCINEX
    98499792 not registered Live/Pending
    RB Health (US) LLC
    2024-04-15
    MUCINEX
    MUCINEX
    90229382 not registered Live/Pending
    RB Health (US) LLC
    2020-10-01
    MUCINEX
    MUCINEX
    88040437 not registered Live/Pending
    Reckitt Benckiser LLC
    2018-07-17
    MUCINEX
    MUCINEX
    86191608 4613098 Live/Registered
    RB HEALTH (US) LLC
    2014-02-12
    MUCINEX
    MUCINEX
    85496330 4168070 Live/Registered
    RB HEALTH (US) LLC
    2011-12-15
    MUCINEX
    MUCINEX
    85489681 4168052 Live/Registered
    RB HEALTH (US) LLC
    2011-12-07
    MUCINEX
    MUCINEX
    77770135 3722363 Live/Registered
    Reckitt Benckiser Inc.
    2009-06-29
    MUCINEX
    MUCINEX
    76297961 2670161 Live/Registered
    RB HEALTH (US) LLC
    2001-08-08
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