NDC 48951-2064

Betula Argentum

Betula Argentum

Betula Argentum is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Uriel Pharmacy Inc.. The primary component is Betula Pubescens Bark; Betula Pubescens Leaf; Apis Mellifera; Formica Rufa; Silver; Arnica Montana.

Product ID48951-2064_6d86672e-b53e-2007-e053-2a91aa0ada70
NDC48951-2064
Product TypeHuman Otc Drug
Proprietary NameBetula Argentum
Generic NameBetula Argentum
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2009-09-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameUriel Pharmacy Inc.
Substance NameBETULA PUBESCENS BARK; BETULA PUBESCENS LEAF; APIS MELLIFERA; FORMICA RUFA; SILVER; ARNICA MONTANA
Active Ingredient Strength1 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 48951-2064-2

1350 PELLET in 1 BOTTLE, GLASS (48951-2064-2)
Marketing Start Date2009-09-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 48951-2064-2 [48951206402]

Betula Argentum PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01

Drug Details

Active Ingredients

IngredientStrength
BETULA PUBESCENS BARK1 [hp_X]/1

OpenFDA Data

SPL SET ID:0d697558-af48-4173-9603-fc2c4bb9915f
Manufacturer
UNII

NDC Crossover Matching brand name "Betula Argentum" or generic name "Betula Argentum"

NDCBrand NameGeneric Name
48951-2063Betula ArgentumBetula Argentum
48951-2064Betula ArgentumBetula Argentum

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