NDC 15631-0194

FERRUM SULPHURICUM

Ferrum Sulphuricum

FERRUM SULPHURICUM 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 Sulfate.

Product ID15631-0194_a130687a-4b81-054f-e053-2995a90af780
NDC15631-0194
Product TypeHuman Otc Drug
Proprietary NameFERRUM SULPHURICUM
Generic NameFerrum Sulphuricum
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 NameFERROUS SULFATE
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0194-0

100 PELLET in 1 PACKAGE (15631-0194-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0194-5 [15631019405]

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

NDC 15631-0194-1 [15631019401]

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

NDC 15631-0194-4 [15631019404]

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

NDC 15631-0194-2 [15631019402]

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

NDC 15631-0194-3 [15631019403]

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

NDC 15631-0194-0 [15631019400]

FERRUM SULPHURICUM 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 SULFATE1 [hp_X]/1

OpenFDA Data

SPL SET ID:1d958ef8-9892-4fc1-8602-a070e9baa4d4
Manufacturer
UNII

NDC Crossover Matching brand name "FERRUM SULPHURICUM" or generic name "Ferrum Sulphuricum"

NDCBrand NameGeneric Name
0220-2111Ferrum sulphuricumFERROUS SULFATE
15631-0194FERRUM SULPHURICUMFERRUM SULPHURICUM
37662-0843Ferrum SulphuricumFerrum Sulphuricum
37662-0844Ferrum SulphuricumFerrum Sulphuricum
37662-0845Ferrum SulphuricumFerrum Sulphuricum
37662-0846Ferrum SulphuricumFerrum Sulphuricum
37662-0847Ferrum SulphuricumFerrum Sulphuricum
37662-0848Ferrum SulphuricumFerrum Sulphuricum
37662-0849Ferrum SulphuricumFerrum Sulphuricum
37662-0850Ferrum SulphuricumFerrum Sulphuricum
68428-941Ferrum sulphuricumFERROUS SULFATE
71919-293Ferrum sulphuricumFERROUS SULFATE

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