NDC 63824-926

Mucinex Allergy

Fexofenadine Hydrochloride

Mucinex Allergy is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Reckitt Benckiser Llc. The primary component is Fexofenadine Hydrochloride.

Product ID63824-926_b87ef385-cbb8-41ae-9cef-e4bf9af038f4
NDC63824-926
Product TypeHuman Otc Drug
Proprietary NameMucinex Allergy
Generic NameFexofenadine Hydrochloride
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2014-01-02
Marketing CategoryANDA / ANDA
Application NumberANDA076502
Labeler NameReckitt Benckiser LLC
Substance NameFEXOFENADINE HYDROCHLORIDE
Active Ingredient Strength180 mg/1
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 63824-926-05

1 BLISTER PACK in 1 CARTON (63824-926-05) > 5 TABLET in 1 BLISTER PACK
Marketing Start Date2014-01-02
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 63824-926-05 [63824092605]

Mucinex Allergy TABLET
Marketing CategoryANDA
Application NumberANDA076502
Product TypeHUMAN OTC DRUG
Marketing Start Date2014-01-02
Inactivation Date2020-01-31

NDC 63824-926-30 [63824092630]

Mucinex Allergy TABLET
Marketing CategoryANDA
Application NumberANDA076502
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2014-01-02
Inactivation Date2020-01-31

NDC 63824-926-80 [63824092680]

Mucinex Allergy TABLET
Marketing CategoryANDA
Application NumberANDA076502
Product TypeHUMAN OTC DRUG
Marketing Start Date2014-01-02
Inactivation Date2020-01-31

NDC 63824-926-88 [63824092688]

Mucinex Allergy TABLET
Marketing CategoryANDA
Application NumberANDA076502
Product TypeHUMAN OTC DRUG
Marketing Start Date2014-04-30
Inactivation Date2020-01-31

NDC 63824-926-40 [63824092640]

Mucinex Allergy TABLET
Marketing CategoryANDA
Application NumberANDA076502
Product TypeHUMAN OTC DRUG
Marketing Start Date2014-01-02
Inactivation Date2020-01-31

NDC 63824-926-10 [63824092610]

Mucinex Allergy TABLET
Marketing CategoryANDA
Application NumberANDA076502
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2014-01-02
Inactivation Date2020-01-31

NDC 63824-926-60 [63824092660]

Mucinex Allergy TABLET
Marketing CategoryANDA
Application NumberANDA076502
Product TypeHUMAN OTC DRUG
Marketing Start Date2014-04-30
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
FEXOFENADINE HYDROCHLORIDE180 mg/1

OpenFDA Data

SPL SET ID:822a1976-97fa-44c6-b12b-f8239af63adf
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1488053
  • 997420

    • Medicade Reported Pricing

    63824092630 MUCINEX ALLERGY 180 MG TABLET

    Pricing Unit: EA | Drug Type:

    63824092610 MUCINEX ALLERGY 180 MG TABLET

    Pricing Unit: EA | Drug Type:

    NDC Crossover Matching brand name "Mucinex Allergy" or generic name "Fexofenadine Hydrochloride"

    NDCBrand NameGeneric Name
    63824-926Mucinex AllergyMucinex Allergy
    10202-107AllergyFexofenadine hydrochloride
    11822-0425allergy relieffexofenadine hydrochloride
    11822-0571allergy relieffexofenadine hydrochloride
    11822-3698Allergy ReliefFexofenadine hydrochloride
    21130-784Allergy ReliefFexofenadine hydrochloride
    0363-0095Fexofenadine hydrochlorideFexofenadine hydrochloride
    0363-0097Fexofenadine hydrochlorideFexofenadine hydrochloride
    0363-0783Fexofenadine hydrochlorideFexofenadine hydrochloride
    0363-9898Fexofenadine HydrochlorideFexofenadine Hydrochloride
    0615-5619Fexofenadine HydrochlorideFexofenadine Hydrochloride
    0615-5620Fexofenadine HydrochlorideFexofenadine Hydrochloride
    0615-7636Fexofenadine HydrochlorideFexofenadine Hydrochloride
    0904-5961Fexofenadine HydrochlorideFexofenadine Hydrochloride
    0904-5962Fexofenadine HydrochlorideFexofenadine Hydrochloride
    0904-5963Fexofenadine HydrochlorideFexofenadine Hydrochloride
    0904-6214fexofenadine hydrochloridefexofenadine hydrochloride
    0904-6711Fexofenadine hydrochlorideFexofenadine hydrochloride
    10202-229Fexofenadine hydrochlorideFexofenadine hydrochloride
    13107-066Fexofenadine hydrochlorideFexofenadine hydrochloride
    13107-067Fexofenadine hydrochlorideFexofenadine hydrochloride
    21695-461Fexofenadine HydrochlorideFexofenadine Hydrochloride
    21695-462Fexofenadine HydrochlorideFexofenadine Hydrochloride
    30142-878Fexofenadine hydrochlorideFexofenadine hydrochloride
    0179-8325Fexofenadine Hydrochloride 180Fexofenadine Hydrochloride
    0113-0571good sense aller easefexofenadine hydrochloride
    0113-0847good sense aller easefexofenadine hydrochloride
    11673-571up and up allergy relieffexofenadine hydrochloride
    11673-617up and up allergy relieffexofenadine hydrochloride
    11673-800up and up allergy reliefFexofenadine Hydrochloride
    0363-0571wal fex allergyfexofenadine hydrochloride
    0363-0784Wal-FexFexofenadine hydrochloride

    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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