NDC 0220-2165

Fucus vesiculosus

Fucus Vesiculosus

Fucus vesiculosus is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Boiron. The primary component is Fucus Vesiculosus.

Product ID0220-2165_85a180d8-01d6-78b8-e053-2991aa0aed90
NDC0220-2165
Product TypeHuman Otc Drug
Proprietary NameFucus vesiculosus
Generic NameFucus Vesiculosus
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date1983-03-03
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameBoiron
Substance NameFUCUS VESICULOSUS
Active Ingredient Strength30 [hp_C]/30[hp_C]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 0220-2165-41

30 [hp_C] in 1 TUBE (0220-2165-41)
Marketing Start Date1983-03-03
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0220-2165-41 [00220216541]

Fucus vesiculosus PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date1983-03-03

Drug Details

Active Ingredients

IngredientStrength
FUCUS VESICULOSUS30 [hp_C]/30[hp_C]

OpenFDA Data

SPL SET ID:85a180d8-01d5-78b8-e053-2991aa0aed90
Manufacturer
UNII

NDC Crossover Matching brand name "Fucus vesiculosus" or generic name "Fucus Vesiculosus"

NDCBrand NameGeneric Name
0220-2165Fucus vesiculosusFUCUS VESICULOSUS
0220-2167Fucus vesiculosusFUCUS VESICULOSUS
15631-0199FUCUS VESICULOSUSFUCUS VESICULOSUS
15631-0587FUCUS VESICULOSUSFUCUS VESICULOSUS
57520-0676Fucus VesiculosusFucus vesiculosus,
60512-6695FUCUS VESICULOSUSFUCUS VESICULOSUS
68428-944Fucus vesiculosusFUCUS VESICULOSUS
71919-304Fucus vesiculosusFUCUS VESICULOSUS
58264-0106D-100Fucus vesiculosus

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