NDC 15631-0189

FERRUM BROMATUM

Ferrum Bromatum

FERRUM BROMATUM 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 Ferrous Bromide.

Product ID15631-0189_833c1030-6404-4905-8667-4b82716ac9b5
NDC15631-0189
Product TypeHuman Otc Drug
Proprietary NameFERRUM BROMATUM
Generic NameFerrum Bromatum
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-10-02
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameFERROUS BROMIDE
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0189-0

100 PELLET in 1 PACKAGE (15631-0189-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0189-4 [15631018904]

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

NDC 15631-0189-3 [15631018903]

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

NDC 15631-0189-0 [15631018900]

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

NDC 15631-0189-2 [15631018902]

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

NDC 15631-0189-1 [15631018901]

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

NDC 15631-0189-5 [15631018905]

FERRUM BROMATUM 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
FERROUS BROMIDE3 [hp_X]/1

OpenFDA Data

SPL SET ID:bdb5d034-6a44-43f6-a931-953926160603
Manufacturer
UNII

NDC Crossover Matching brand name "FERRUM BROMATUM" or generic name "Ferrum Bromatum"

NDCBrand NameGeneric Name
15631-0189FERRUM BROMATUMFERRUM BROMATUM
37662-0650Ferrum BromatumFerrum Bromatum
37662-0651Ferrum BromatumFerrum Bromatum
37662-0652Ferrum BromatumFerrum Bromatum
37662-0653Ferrum BromatumFerrum Bromatum
37662-0654Ferrum BromatumFerrum Bromatum
37662-0655Ferrum BromatumFerrum Bromatum
37662-0656Ferrum BromatumFerrum Bromatum
63545-659Ferrum BromatumFerrum Bromatum

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