NDC 15631-0200

GALANTHUS NIVALIS

Galanthus Nivalis

GALANTHUS NIVALIS 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 Galanthus Nivalis.

Product ID15631-0200_736cf117-3830-4767-a63f-5e46e3e8446b
NDC15631-0200
Product TypeHuman Otc Drug
Proprietary NameGALANTHUS NIVALIS
Generic NameGalanthus Nivalis
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-10-25
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameGALANTHUS NIVALIS
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0200-0

100 PELLET in 1 PACKAGE (15631-0200-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0200-0 [15631020000]

GALANTHUS NIVALIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0200-3 [15631020003]

GALANTHUS NIVALIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0200-2 [15631020002]

GALANTHUS NIVALIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0200-1 [15631020001]

GALANTHUS NIVALIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0200-5 [15631020005]

GALANTHUS NIVALIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0200-4 [15631020004]

GALANTHUS NIVALIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

Drug Details

Active Ingredients

IngredientStrength
GALANTHUS NIVALIS1 [hp_X]/1

OpenFDA Data

SPL SET ID:94989da1-3220-4434-bf1d-03b553707285
Manufacturer
UNII

NDC Crossover Matching brand name "GALANTHUS NIVALIS" or generic name "Galanthus Nivalis"

NDCBrand NameGeneric Name
15631-0200GALANTHUS NIVALISGALANTHUS NIVALIS
68428-395Galanthus nivalisGALANTHUS NIVALIS
71919-305Galanthus nivalisGALANTHUS NIVALIS

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