NDC 71919-287

Ferrum carbonicum

Ferrous Carbonate

Ferrum carbonicum is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Washington Homeopathic Products. The primary component is Ferrous Carbonate.

Product ID71919-287_7e4e7e58-41ab-89a2-e053-2a91aa0a790b
NDC71919-287
Product TypeHuman Otc Drug
Proprietary NameFerrum carbonicum
Generic NameFerrous Carbonate
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2011-05-11
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameWashington Homeopathic Products
Substance NameFERROUS CARBONATE
Active Ingredient Strength30 [hp_C]/mL
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 71919-287-07

15 mL in 1 VIAL, GLASS (71919-287-07)
Marketing Start Date2011-05-11
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71919-287-08 [71919028708]

Ferrum carbonicum LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-05-11

NDC 71919-287-09 [71919028709]

Ferrum carbonicum LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-05-11

NDC 71919-287-07 [71919028707]

Ferrum carbonicum LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-05-11

NDC 71919-287-10 [71919028710]

Ferrum carbonicum LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-05-11

Drug Details

Active Ingredients

IngredientStrength
FERROUS CARBONATE30 [hp_C]/mL

OpenFDA Data

SPL SET ID:10810575-b0fb-452e-8b54-81e33e65e5b4
Manufacturer
UNII

NDC Crossover Matching brand name "Ferrum carbonicum" or generic name "Ferrous Carbonate"

NDCBrand NameGeneric Name
53645-1750Ferrum CarbonicumFerrum Carbonicum
68428-381Ferrum carbonicumFERROUS CARBONATE
71919-287Ferrum carbonicumFERROUS CARBONATE

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.