NDC 15631-0171

DROSERA ROTUNDIFOLIA

Drosera Rotundifolia

DROSERA ROTUNDIFOLIA is a Oral Pellet 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 ID15631-0171_7ffbc5b9-1cf5-4716-9bdd-891f257ab9f5
NDC15631-0171
Product TypeHuman Otc Drug
Proprietary NameDROSERA ROTUNDIFOLIA
Generic NameDrosera Rotundifolia
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-10-02
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 15631-0171-0

100 PELLET in 1 PACKAGE (15631-0171-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0171-1 [15631017101]

DROSERA ROTUNDIFOLIA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-19

NDC 15631-0171-0 [15631017100]

DROSERA ROTUNDIFOLIA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-19

NDC 15631-0171-2 [15631017102]

DROSERA ROTUNDIFOLIA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-19

NDC 15631-0171-3 [15631017103]

DROSERA ROTUNDIFOLIA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-19

NDC 15631-0171-4 [15631017104]

DROSERA ROTUNDIFOLIA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-19

NDC 15631-0171-5 [15631017105]

DROSERA ROTUNDIFOLIA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-19

Drug Details

Active Ingredients

IngredientStrength
DROSERA ROTUNDIFOLIA1 [hp_X]/1

OpenFDA Data

SPL SET ID:10fb8cba-e5bd-48c0-b2b5-64bd1a23fd7a
Manufacturer
UNII

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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