NDC 0220-7838

Syphilinum

Treponemic Skin Canker Human

Syphilinum is a Oral Pellet in the Human Prescription Drug category. It is labeled and distributed by Boiron. The primary component is Treponemic Skin Canker Human.

Product ID0220-7838_8771de7e-b059-ea00-e053-2a95a90a7512
NDC0220-7838
Product TypeHuman Prescription Drug
Proprietary NameSyphilinum
Generic NameTreponemic Skin Canker Human
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date1983-03-03
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameBoiron
Substance NameTREPONEMIC SKIN CANKER HUMAN
Active Ingredient Strength30 [hp_C]/30[hp_C]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 0220-7838-41

30 [hp_C] in 1 TUBE (0220-7838-41)
Marketing Start Date1983-03-03
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0220-7838-41 [00220783841]

Syphilinum PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1983-03-03

Drug Details

Active Ingredients

IngredientStrength
TREPONEMIC SKIN CANKER HUMAN30 [hp_C]/30[hp_C]

NDC Crossover Matching brand name "Syphilinum" or generic name "Treponemic Skin Canker Human"

NDCBrand NameGeneric Name
0220-7838SyphilinumTREPONEMIC SKIN CANKER HUMAN
64117-408SYPHILINUMTREPONEMIC SKIN CANKER HUMAN
62106-6861LUESINUMSyphilinum
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