United States · FDA National Drug Code directory
Angiplex
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 62106-1229_ed11e5b0-cdb3-1f9a-e053-2995a90a0f16
- Product NDC
- 62106-1229
- Form
- TABLET
- Composition / generic term
- Arum triphyllum, Aconitum napellus, Apis mellifica, Belladonna, Phytolacca decandra, Kali bichromicum, Lachesis mutus, Mercurius solubilis
- Labeler
- Seroyal USA
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start / end (source format)
- 20150119
- Source listing expiry
- 20261231
Source-listed ingredients
- ARISAEMA TRIPHYLLUM ROOT — 4 [hp_X]/1
- ACONITUM NAPELLUS — 8 [hp_X]/1
- APIS MELLIFERA — 8 [hp_X]/1
- ATROPA BELLADONNA — 8 [hp_X]/1
- PHYTOLACCA AMERICANA ROOT — 8 [hp_X]/1
- POTASSIUM DICHROMATE — 10 [hp_X]/1
- LACHESIS MUTA VENOM — 10 [hp_X]/1
- MERCURIUS SOLUBILIS — 10 [hp_X]/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BLISTER PACK in 1 BOX (62106-1229-3) / 30 TABLET in 1 BLISTER PACK · 62106-1229-3
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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