NDC 0220-3189

Lycopus virginicus

Lycopus Virginicus

Lycopus virginicus is a Oral Pellet in the Human Prescription Drug category. It is labeled and distributed by Boiron. The primary component is Lycopus Virginicus.

Product ID0220-3189_8749dd83-0cbe-66e3-e053-2a95a90aac10
NDC0220-3189
Product TypeHuman Prescription Drug
Proprietary NameLycopus virginicus
Generic NameLycopus Virginicus
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date1983-03-03
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameBoiron
Substance NameLYCOPUS VIRGINICUS
Active Ingredient Strength6 [hp_C]/6[hp_C]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 0220-3189-41

6 [hp_C] in 1 TUBE (0220-3189-41)
Marketing Start Date1983-03-03
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0220-3189-41 [00220318941]

Lycopus virginicus PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1983-03-03

Drug Details

Active Ingredients

IngredientStrength
LYCOPUS VIRGINICUS6 [hp_C]/6[hp_C]

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
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.