NDC 52389-241

Uricalm Maximum Strength

Phenazopyridine Hydochloride

Uricalm Maximum Strength is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by Alva-amco Pharmacal Companies, Inc.. The primary component is Phenazopyridine Hydrochloride.

Product ID52389-241_7898772c-4194-ba76-e053-2991aa0a4990
NDC52389-241
Product TypeHuman Otc Drug
Proprietary NameUricalm Maximum Strength
Generic NamePhenazopyridine Hydochloride
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2008-04-29
Marketing CategoryUNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
Labeler NameAlva-Amco Pharmacal Companies, Inc.
Substance NamePHENAZOPYRIDINE HYDROCHLORIDE
Active Ingredient Strength100 mg/1
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 52389-241-24

1 BLISTER PACK in 1 CARTON (52389-241-24) > 24 TABLET, FILM COATED in 1 BLISTER PACK (52389-241-01)
Marketing Start Date2008-04-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 52389-241-04 [52389024104]

Uricalm Maximum Strength TABLET, FILM COATED
Marketing Categoryunapproved drug other
Product TypeHUMAN OTC DRUG
Marketing Start Date2014-02-26

NDC 52389-241-03 [52389024103]

Uricalm Maximum Strength TABLET, FILM COATED
Marketing Categoryunapproved drug other
Product TypeHUMAN OTC DRUG
Marketing Start Date2008-04-29

NDC 52389-241-12 [52389024112]

Uricalm Maximum Strength TABLET, FILM COATED
Marketing Categoryunapproved drug other
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-08-01
Marketing End Date2011-12-31

NDC 52389-241-02 [52389024102]

Uricalm Maximum Strength TABLET, FILM COATED
Marketing Categoryunapproved drug other
Product TypeHUMAN OTC DRUG
Marketing Start Date2008-04-29

NDC 52389-241-28 [52389024128]

Uricalm Maximum Strength TABLET, FILM COATED
Marketing Categoryunapproved drug other
Product TypeHUMAN OTC DRUG
Marketing Start Date2014-02-20

NDC 52389-241-01 [52389024101]

Uricalm Maximum Strength TABLET, FILM COATED
Marketing Categoryunapproved drug other
Product TypeHUMAN OTC DRUG
Marketing Start Date2008-04-29

NDC 52389-241-24 [52389024124]

Uricalm Maximum Strength TABLET, FILM COATED
Marketing Categoryunapproved drug other
Product TypeHUMAN OTC DRUG
Marketing Start Date2008-04-29

NDC 52389-241-36 [52389024136]

Uricalm Maximum Strength TABLET, FILM COATED
Marketing Categoryunapproved drug other
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-07-15
Marketing End Date2013-06-15

Drug Details

Active Ingredients

IngredientStrength
PHENAZOPYRIDINE HYDROCHLORIDE99.5 mg/1

OpenFDA Data

SPL SET ID:1d94b45c-ee0b-499d-aca2-e8cd8dd490d2
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1094147
  • 1094149
    • UPC Code
  • 0072959415242

    • Trademark Results [Uricalm]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    URICALM
    URICALM
    98574225 not registered Live/Pending
    Kobayashi Pharmaceutical Co., Ltd.
    2024-05-29
    URICALM
    URICALM
    97358730 not registered Live/Pending
    Alva-Amco Pharmacal Companies, LLC.
    2022-04-12
    URICALM
    URICALM
    78521321 not registered Dead/Abandoned
    Alva International LLC
    2004-11-22
    URICALM
    URICALM
    77075585 3285348 Live/Registered
    ALVA-AMCO PHARMACAL COS., INC.
    2007-01-03
    URICALM
    URICALM
    75662348 not registered Dead/Abandoned
    STANDARD HOMEOPATHIC COMPANY, INC.
    1999-03-17
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