Erbium Sulphuricum

Product NDC
37662-2920
Type
HUMAN OTC DRUG
Nonproprietary name
Erbium Sulphuricum
Dosage form
PELLET
Route
ORAL
Labeler
Hahnemann Laboratories, INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Substance
ERBIUM SULFATE OCTAHYDRATE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
37662-2920-180 PELLET in 1 VIAL, GLASS (37662-2920-1) 2023-04-05NoHistorical
37662-2920-2200 PELLET in 1 VIAL, GLASS (37662-2920-2) 2023-04-05NoHistorical
37662-2920-31200 PELLET in 1 BOTTLE, GLASS (37662-2920-3) 2023-04-05NoHistorical
37662-2920-44000 PELLET in 1 BOTTLE, GLASS (37662-2920-4) 2023-04-05NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Erbium Sulphuricum - Hahnemann Laboratories, INC.Hahnemann Laboratories, INC.2023-04-05HUMAN OTC DRUG LABEL1