NDC 15631-0288

MELILOTUS OFFICINALIS

Melilotus Officinalis

MELILOTUS OFFICINALIS is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Rxhomeo Private Limited D.b.a. Rxhomeo, Inc. The primary component is Melilotus Officinalis Top.

Product ID15631-0288_1f974da6-2b45-4a75-992e-f858eab445a5
NDC15631-0288
Product TypeHuman Otc Drug
Proprietary NameMELILOTUS OFFICINALIS
Generic NameMelilotus Officinalis
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-09-09
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameMELILOTUS OFFICINALIS TOP
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0288-0

100 PELLET in 1 PACKAGE (15631-0288-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0288-4 [15631028804]

MELILOTUS OFFICINALIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0288-0 [15631028800]

MELILOTUS OFFICINALIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0288-2 [15631028802]

MELILOTUS OFFICINALIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0288-1 [15631028801]

MELILOTUS OFFICINALIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0288-5 [15631028805]

MELILOTUS OFFICINALIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0288-3 [15631028803]

MELILOTUS OFFICINALIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

Drug Details

Active Ingredients

IngredientStrength
MELILOTUS OFFICINALIS TOP3 [hp_X]/1

OpenFDA Data

SPL SET ID:e4285a30-e451-428f-bc47-0b5cd6369ec2
Manufacturer
UNII

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

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