Melilotus Alba

Product NDC
37662-2495
Type
HUMAN OTC DRUG
Nonproprietary name
Melilotus Alba
Dosage form
PELLET
Route
ORAL
Labeler
Hahnemann Laboratories, INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Substance
MELILOTUS ALBUS TOP
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
37662-2495-180 PELLET in 1 VIAL, GLASS (37662-2495-1) 2023-01-25NoHistorical
37662-2495-2200 PELLET in 1 VIAL, GLASS (37662-2495-2) 2023-01-25NoHistorical
37662-2495-31200 PELLET in 1 BOTTLE, GLASS (37662-2495-3) 2023-01-25NoHistorical
37662-2495-44000 PELLET in 1 BOTTLE, GLASS (37662-2495-4) 2023-01-25NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Melilotus Alba - Hahnemann Laboratories, INC.Hahnemann Laboratories, INC.2023-01-25HUMAN OTC DRUG LABEL1