NDC 48951-2063

Betula Argentum

Betula Argentum

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

Product ID48951-2063_6a85cd07-ce72-550a-e053-2991aa0ae511
NDC48951-2063
Product TypeHuman Otc Drug
Proprietary NameBetula Argentum
Generic NameBetula Argentum
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2009-09-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameUriel Pharmacy Inc.
Substance NameAPIS MELLIFERA; BETULA PUBESCENS BARK; BETULA PUBESCENS LEAF; FORMICA RUFA; SILVER; ARNICA MONTANA
Active Ingredient Strength3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 48951-2063-1

10 AMPULE in 1 BOX (48951-2063-1) > 1 mL in 1 AMPULE
Marketing Start Date2009-09-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 48951-2063-1 [48951206301]

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

Drug Details

Active Ingredients

IngredientStrength
APIS MELLIFERA3 [hp_X]/mL

OpenFDA Data

SPL SET ID:7f436fc5-0983-4ce3-9951-e68e395bcab0
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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