NDC 15631-0185

FAGOPYRUM ESCULENTUM

Fagopyrum Esculentum

FAGOPYRUM ESCULENTUM 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 Fagopyrum Esculentum.

Product ID15631-0185_a11ae4a3-a712-6233-e053-2a95a90a51b6
NDC15631-0185
Product TypeHuman Otc Drug
Proprietary NameFAGOPYRUM ESCULENTUM
Generic NameFagopyrum Esculentum
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 NameFAGOPYRUM ESCULENTUM
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0185-0

100 PELLET in 1 PACKAGE (15631-0185-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0185-2 [15631018502]

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

NDC 15631-0185-4 [15631018504]

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

NDC 15631-0185-3 [15631018503]

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

NDC 15631-0185-5 [15631018505]

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

NDC 15631-0185-0 [15631018500]

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

NDC 15631-0185-1 [15631018501]

FAGOPYRUM ESCULENTUM 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
FAGOPYRUM ESCULENTUM1 [hp_X]/1

OpenFDA Data

SPL SET ID:d614221e-244b-4ba1-b7fc-2fd08defdaaf
Manufacturer
UNII

NDC Crossover Matching brand name "FAGOPYRUM ESCULENTUM" or generic name "Fagopyrum Esculentum"

NDCBrand NameGeneric Name
0220-2045Fagopyrum esculentumFAGOPYRUM ESCULENTUM
15631-0185FAGOPYRUM ESCULENTUMFAGOPYRUM ESCULENTUM
68428-378Fagopyrum esculentumFAGOPYRUM ESCULENTUM
71919-283Fagopyrum esculentumFAGOPYRUM ESCULENTUM
0268-6113BUCKWHEATFAGOPYRUM ESCULENTUM
22840-5709BuckwheatFagopyrum esculentum
64117-228ITCHY SKIN RUNNY NOSEFAGOPYRUM ESCULENTUM

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