NDC 15631-0451

USTILAGO MAIDIS

Ustilago Maidis

USTILAGO MAIDIS 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 Ustilago Maydis.

Product ID15631-0451_8f3404a8-8354-4028-91f5-9670f5dadaf0
NDC15631-0451
Product TypeHuman Otc Drug
Proprietary NameUSTILAGO MAIDIS
Generic NameUstilago Maidis
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-10-31
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameUSTILAGO MAYDIS
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0451-0

100 PELLET in 1 VIAL, SINGLE-DOSE (15631-0451-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0451-2 [15631045102]

USTILAGO MAIDIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0451-4 [15631045104]

USTILAGO MAIDIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0451-5 [15631045105]

USTILAGO MAIDIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0451-0 [15631045100]

USTILAGO MAIDIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0451-1 [15631045101]

USTILAGO MAIDIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0451-3 [15631045103]

USTILAGO MAIDIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

Drug Details

Active Ingredients

IngredientStrength
USTILAGO MAYDIS3 [hp_X]/1

OpenFDA Data

SPL SET ID:58edaa86-58f9-45dc-95ac-23a20b26e2fd
Manufacturer
UNII

NDC Crossover Matching brand name "USTILAGO MAIDIS" or generic name "Ustilago Maidis"

NDCBrand NameGeneric Name
0220-5153USTILAGO MAIDISUSTILAGO MAYDIS
0220-5156Ustilago maidisUSTILAGO MAYDIS
15631-0451USTILAGO MAIDISUSTILAGO MAIDIS
37662-2106Ustilago MaidisUstilago Maidis
37662-2107Ustilago MaidisUstilago Maidis
37662-2108Ustilago MaidisUstilago Maidis
37662-2109Ustilago MaidisUstilago Maidis
37662-2110Ustilago MaidisUstilago Maidis
37662-2111Ustilago MaidisUstilago Maidis
37662-2112Ustilago MaidisUstilago Maidis
37662-2113Ustilago MaidisUstilago Maidis
37662-2114Ustilago MaidisUstilago Maidis
68428-690Ustilago maidisUSTILAGO MAYDIS
71919-699USTILAGO MAIDISUstilago maydis

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