Angiplex

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerSeroyal USA

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
6210612293
1 BLISTER PACK in 1 BOX (62106-1229-3) / 30 TABLET in 1 BLISTER PACK

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Raw payload (JSON)

{
  "route": "SUBLINGUAL",
  "productid": "62106-1229_ed11e5b0-cdb3-1f9a-e053-2995a90a0f16",
  "productndc": "62106-1229",
  "dosage_form": "TABLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ACONITUM NAPELLUS; APIS MELLIFERA; ARISAEMA TRIPHYLLUM ROOT; ATROPA BELLADONNA; LACHESIS MUTA VENOM; MERCURIUS SOLUBILIS; PHYTOLACCA AMERICANA ROOT; POTASSIUM DICHROMATE",
  "proprietary_name": "Angiplex",
  "active_ingred_unit": "[hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Arum triphyllum, Aconitum napellus, Apis mellifica, Belladonna, Phytolacca decandra, Kali bichromicum, Lachesis mutus, Mercurius solubilis",
  "start_marketing_date": "20150119",
  "active_numerator_strength": "8; 8; 4; 8; 10; 10; 8; 10"
}

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