NDC 15631-0279

LYCOPUS VIRGINICUS

Lycopus Virginicus

LYCOPUS VIRGINICUS 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 Lycopus Virginicus.

Product ID15631-0279_a185c9c8-aaad-0e63-e053-2995a90a1b1e
NDC15631-0279
Product TypeHuman Otc Drug
Proprietary NameLYCOPUS VIRGINICUS
Generic NameLycopus Virginicus
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-09-07
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameLYCOPUS VIRGINICUS
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0279-0

100 PELLET in 1 PACKAGE (15631-0279-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0279-2 [15631027902]

LYCOPUS VIRGINICUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0279-3 [15631027903]

LYCOPUS VIRGINICUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0279-1 [15631027901]

LYCOPUS VIRGINICUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0279-4 [15631027904]

LYCOPUS VIRGINICUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0279-5 [15631027905]

LYCOPUS VIRGINICUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0279-0 [15631027900]

LYCOPUS VIRGINICUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

Drug Details

Active Ingredients

IngredientStrength
LYCOPUS VIRGINICUS1 [hp_X]/1

OpenFDA Data

SPL SET ID:430e9dff-919d-42b5-ace0-42ef427abecf
Manufacturer
UNII

NDC Crossover Matching brand name "LYCOPUS VIRGINICUS" or generic name "Lycopus Virginicus"

NDCBrand NameGeneric Name
0220-3189Lycopus virginicusLYCOPUS VIRGINICUS
0220-3194Lycopus virginicusLYCOPUS VIRGINICUS
15631-0279LYCOPUS VIRGINICUSLYCOPUS VIRGINICUS
15631-0628LYCOPUS VIRGINICUSLYCOPUS VIRGINICUS
37662-1037Lycopus VirginicusLycopus Virginicus
37662-1038Lycopus VirginicusLycopus Virginicus
37662-1039Lycopus VirginicusLycopus Virginicus
37662-1040Lycopus VirginicusLycopus Virginicus
37662-1041Lycopus VirginicusLycopus Virginicus
37662-1042Lycopus VirginicusLycopus Virginicus
37662-1043Lycopus VirginicusLycopus Virginicus
37662-1044Lycopus VirginicusLycopus Virginicus
68428-486Lycopus virginicusLYCOPUS VIRGINICUS
71919-430Lycopus virginicusLYCOPUS VIRGINICUS
64117-258COUGH HEADACHELYCOPUS VIRGINICUS

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