NDC 62106-1229

Angiplex

Arum Triphyllum, Aconitum Napellus, Apis Mellifica, Belladonna, Phytolacca Decandra, Kali Bichromicum, Lachesis Mutus, Mercurius Solubilis

Angiplex is a Sublingual Tablet in the Human Otc Drug category. It is labeled and distributed by Seroyal Usa. The primary component is Arisaema Triphyllum Root; Aconitum Napellus; Apis Mellifera; Atropa Belladonna; Phytolacca Americana Root; Potassium Dichromate; Lachesis Muta Venom; Mercurius Solubilis.

Product ID62106-1229_6fa6a261-5148-3151-e053-2991aa0ae4e6
NDC62106-1229
Product TypeHuman Otc Drug
Proprietary NameAngiplex
Generic NameArum Triphyllum, Aconitum Napellus, Apis Mellifica, Belladonna, Phytolacca Decandra, Kali Bichromicum, Lachesis Mutus, Mercurius Solubilis
Dosage FormTablet
Route of AdministrationSUBLINGUAL
Marketing Start Date2015-01-19
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameSeroyal USA
Substance NameARISAEMA TRIPHYLLUM ROOT; ACONITUM NAPELLUS; APIS MELLIFERA; ATROPA BELLADONNA; PHYTOLACCA AMERICANA ROOT; POTASSIUM DICHROMATE; LACHESIS MUTA VENOM; MERCURIUS SOLUBILIS
Active Ingredient Strength4 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 62106-1229-3

1 BLISTER PACK in 1 BOX (62106-1229-3) > 30 TABLET in 1 BLISTER PACK
Marketing Start Date2015-01-19
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 62106-1229-3 [62106122903]

Angiplex TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-01-19

Drug Details

Active Ingredients

IngredientStrength
ARISAEMA TRIPHYLLUM ROOT4 [hp_X]/1

OpenFDA Data

SPL SET ID:0d04b1a0-6c43-5f25-e054-00144ff8d46c
Manufacturer
UNII
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