NDC 37662-1145

Melilotus Officinalis

Melilotus Officinalis

Melilotus Officinalis is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Hahnemann Laboratories, Inc.. The primary component is Melilotus Officinalis Top.

Product ID37662-1145_e537e1fc-3b8a-8ce1-e053-2a95a90a8005
NDC37662-1145
Product TypeHuman Otc Drug
Proprietary NameMelilotus Officinalis
Generic NameMelilotus Officinalis
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2022-08-01
Marketing CategoryUNAPPROVED HOMEOPATHIC /
Labeler NameHahnemann Laboratories, INC.
Substance NameMELILOTUS OFFICINALIS TOP
Active Ingredient Strength1 [hp_M]/1
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 37662-1145-1

200 PELLET in 1 VIAL, GLASS (37662-1145-1)
Marketing Start Date2022-08-01
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "Melilotus Officinalis" or generic name "Melilotus Officinalis"

NDCBrand NameGeneric Name
0220-3335Melilotus officinalisMELILOTUS OFFICINALIS TOP
15631-0288MELILOTUS OFFICINALISMELILOTUS OFFICINALIS
37662-1139Melilotus OfficinalisMelilotus Officinalis
37662-1140Melilotus OfficinalisMelilotus Officinalis
37662-1141Melilotus OfficinalisMelilotus Officinalis
37662-1142Melilotus OfficinalisMelilotus Officinalis
37662-1143Melilotus OfficinalisMelilotus Officinalis
37662-1144Melilotus OfficinalisMelilotus Officinalis
37662-1145Melilotus OfficinalisMelilotus Officinalis
37662-1146Melilotus OfficinalisMelilotus Officinalis
68428-497Melilotus officinalisMELILOTUS OFFICINALIS TOP
71919-447Melilotus officinalisMELILOTUS OFFICINALIS TOP

© 2022 FDA.report
This site is not affiliated with or endorsed by the FDA.