NDC 15631-0197

FORMICA RUFA

Formica Rufa

FORMICA RUFA 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 Formica Rufa.

Product ID15631-0197_206131ac-4216-454c-8b0f-629ee75f2eb4
NDC15631-0197
Product TypeHuman Otc Drug
Proprietary NameFORMICA RUFA
Generic NameFormica Rufa
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 NameFORMICA RUFA
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0197-0

100 PELLET in 1 PACKAGE (15631-0197-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0197-4 [15631019704]

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

NDC 15631-0197-0 [15631019700]

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

NDC 15631-0197-2 [15631019702]

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

NDC 15631-0197-5 [15631019705]

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

NDC 15631-0197-3 [15631019703]

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

NDC 15631-0197-1 [15631019701]

FORMICA RUFA 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
FORMICA RUFA1 [hp_X]/1

OpenFDA Data

SPL SET ID:d79797b9-e102-4920-b565-6185a46c15e2
Manufacturer
UNII

NDC Crossover Matching brand name "FORMICA RUFA" or generic name "Formica Rufa"

NDCBrand NameGeneric Name
0220-2139Formica rufaFORMICA RUFA
0220-2140Formica rufaFORMICA RUFA
15631-0197FORMICA RUFAFORMICA RUFA
37662-0733Formica RufaFormica Rufa
37662-0734Formica RufaFormica Rufa
37662-0735Formica RufaFormica Rufa
37662-0736Formica RufaFormica Rufa
37662-0737Formica RufaFormica Rufa
37662-0738Formica RufaFormica Rufa
37662-0739Formica RufaFormica Rufa
37662-0740Formica RufaFormica Rufa
62106-6633FORMICA RUFARed ant
68428-391Formica rufaFORMICA RUFA
71919-299Formica rufaFORMICA RUFA

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