NDC 15631-0446

TRIFOLIUM PRATENSE

Trifolium Pratense

TRIFOLIUM PRATENSE 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 Juniperus Sabina Leafy Twig.

Product ID15631-0446_a1d2e23b-cec9-599f-e053-2a95a90abc1d
NDC15631-0446
Product TypeHuman Otc Drug
Proprietary NameTRIFOLIUM PRATENSE
Generic NameTrifolium Pratense
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-11-02
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameJUNIPERUS SABINA LEAFY TWIG
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0446-0

100 PELLET in 1 VIAL, SINGLE-DOSE (15631-0446-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0446-5 [15631044605]

TRIFOLIUM PRATENSE PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0446-4 [15631044604]

TRIFOLIUM PRATENSE PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0446-0 [15631044600]

TRIFOLIUM PRATENSE PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0446-2 [15631044602]

TRIFOLIUM PRATENSE PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0446-3 [15631044603]

TRIFOLIUM PRATENSE PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0446-1 [15631044601]

TRIFOLIUM PRATENSE PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

Drug Details

Active Ingredients

IngredientStrength
JUNIPERUS SABINA LEAFY TWIG1 [hp_X]/1

OpenFDA Data

SPL SET ID:e70ce49e-e8a4-491f-913d-b358a2f9126f
Manufacturer
UNII

NDC Crossover Matching brand name "TRIFOLIUM PRATENSE" or generic name "Trifolium Pratense"

NDCBrand NameGeneric Name
15631-0446TRIFOLIUM PRATENSETRIFOLIUM PRATENSE
68428-683Trifolium pratenseTRIFOLIUM PRATENSE FLOWER
71919-686TRIFOLIUM PRATENSETtrifolium pratense
22840-1514Red CloverTrifolium pratense
22840-1515Red CloverTrifolium pratense
22840-1565Red CloverTrifolium pratense
22840-5506Red CloverTrifolium pratense

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