NDC 15631-0575

DROSERA ROTUNDIFOLIA

Drosera Rotundifolia

DROSERA ROTUNDIFOLIA 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 Drosera Rotundifolia.

Product ID15631-0575_070feb38-5117-4d89-b384-8ec811a09562
NDC15631-0575
Product TypeHuman Otc Drug
Proprietary NameDROSERA ROTUNDIFOLIA
Generic NameDrosera Rotundifolia
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2015-12-27
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameDROSERA ROTUNDIFOLIA
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0575-7

10000 TABLET in 1 CONTAINER (15631-0575-7)
Marketing Start Date2015-12-27
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0575-3 [15631057503]

DROSERA ROTUNDIFOLIA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0575-5 [15631057505]

DROSERA ROTUNDIFOLIA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0575-4 [15631057504]

DROSERA ROTUNDIFOLIA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0575-1 [15631057501]

DROSERA ROTUNDIFOLIA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0575-6 [15631057506]

DROSERA ROTUNDIFOLIA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0575-7 [15631057507]

DROSERA ROTUNDIFOLIA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0575-0 [15631057500]

DROSERA ROTUNDIFOLIA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0575-2 [15631057502]

DROSERA ROTUNDIFOLIA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
DROSERA ROTUNDIFOLIA1 [hp_X]/1

OpenFDA Data

SPL SET ID:0af36677-28a7-4e1f-b1c0-a7146cf1b6c4
Manufacturer
UNII
UPC Code
  • 8907460005526
  • NDC Crossover Matching brand name "DROSERA ROTUNDIFOLIA" or generic name "Drosera Rotundifolia"

    NDCBrand NameGeneric Name
    0220-1791Drosera rotundifoliaDROSERA ROTUNDIFOLIA
    15631-0171DROSERA ROTUNDIFOLIADROSERA ROTUNDIFOLIA
    15631-0575DROSERA ROTUNDIFOLIADROSERA ROTUNDIFOLIA
    37662-0642Drosera RotundifoliaDrosera Rotundifolia
    37662-0643Drosera RotundifoliaDrosera Rotundifolia
    37662-0644Drosera RotundifoliaDrosera Rotundifolia
    37662-0645Drosera RotundifoliaDrosera Rotundifolia
    37662-0646Drosera RotundifoliaDrosera Rotundifolia
    37662-0647Drosera RotundifoliaDrosera Rotundifolia
    37662-0648Drosera RotundifoliaDrosera Rotundifolia
    37662-0649Drosera RotundifoliaDrosera Rotundifolia
    60512-1015DROSERA ROTUNDIFOLIADROSERA ROTUNDIFOLIA
    68428-359Drosera rotundifoliaDROSERA ROTUNDIFOLIA
    71919-259Drosera rotundifoliaDROSERA ROTUNDIFOLIA
    0220-1784DroseraDROSERA ROTUNDIFOLIA
    0220-1785DroseraDROSERA ROTUNDIFOLIA
    0220-1788DroseraDROSERA ROTUNDIFOLIA
    0220-1792DroseraDROSERA ROTUNDIFOLIA
    0220-1793DroseraDROSERA ROTUNDIFOLIA
    0220-1796DroseraDROSERA ROTUNDIFOLIA
    0220-1797DroseraDROSERA ROTUNDIFOLIA
    0220-1800DroseraDROSERA ROTUNDIFOLIA
    0220-1801DroseraDROSERA ROTUNDIFOLIA
    68428-142Drosera Rotundifolia Kit RefillDROSERA ROTUNDIFOLIA
    71919-761Drosera Rotundifolia Kit RefillDROSERA ROTUNDIFOLIA
    64117-969Spasmodic CoughDROSERA ROTUNDIFOLIA

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