NDC 15631-0535

BARYTA MURIATICA

Baryta Muriatica

BARYTA MURIATICA is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Rxhomeo Private Limited D.b.a. Rxhomeo, Inc. The primary component is Barium Chloride Dihydrate.

Product ID15631-0535_a12ddb81-dcd6-4748-8da5-81663d5ae7af
NDC15631-0535
Product TypeHuman Otc Drug
Proprietary NameBARYTA MURIATICA
Generic NameBaryta Muriatica
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2015-12-30
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameBARIUM CHLORIDE DIHYDRATE
Active Ingredient Strength6 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0535-5

500 TABLET in 1 CONTAINER (15631-0535-5)
Marketing Start Date2015-12-30
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0535-0 [15631053500]

BARYTA MURIATICA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0535-2 [15631053502]

BARYTA MURIATICA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0535-7 [15631053507]

BARYTA MURIATICA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0535-6 [15631053506]

BARYTA MURIATICA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0535-5 [15631053505]

BARYTA MURIATICA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0535-4 [15631053504]

BARYTA MURIATICA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0535-1 [15631053501]

BARYTA MURIATICA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0535-3 [15631053503]

BARYTA MURIATICA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
BARIUM CHLORIDE DIHYDRATE6 [hp_X]/1

OpenFDA Data

SPL SET ID:1683a3a6-a076-4bf2-9354-d23069631ea6
Manufacturer
UNII
UPC Code
  • 8907460005526
  • NDC Crossover Matching brand name "BARYTA MURIATICA" or generic name "Baryta Muriatica"

    NDCBrand NameGeneric Name
    0220-0755Baryta muriaticaBARIUM CHLORIDE DIHYDRATE
    0220-0756Baryta muriaticaBARIUM CHLORIDE DIHYDRATE
    0220-0793Baryta muriaticaBARIUM CHLORIDE DIHYDRATE
    15631-0075BARYTA MURIATICABARYTA MURIATICA
    15631-0535BARYTA MURIATICABARYTA MURIATICA
    63545-396Baryta MuriaticaBaryta Muriatica
    63545-397Baryta MuriaticaBaryta Muriatica
    63545-398Baryta MuriaticaBaryta Muriatica
    63545-399Baryta MuriaticaBaryta Muriatica
    63545-400Baryta MuriaticaBaryta Muriatica
    63545-401Baryta MuriaticaBaryta Muriatica
    63545-402Baryta MuriaticaBaryta Muriatica
    63545-403Baryta MuriaticaBaryta Muriatica
    68428-250Baryta muriaticaBARIUM CHLORIDE DIHYDRATE
    71919-113Baryta muriaticaBARIUM CHLORIDE DIHYDRATE

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