NDC 15631-0586

FRAXINUS AMERICANA

Fraxinus Americana

FRAXINUS AMERICANA is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Rxhomeo Private Limited D.b.a. Rxhomeo, Inc. The primary component is Fraxinus Americana Bark.

Product ID15631-0586_25449080-d5bd-49e9-ad40-8aa8f0f59164
NDC15631-0586
Product TypeHuman Otc Drug
Proprietary NameFRAXINUS AMERICANA
Generic NameFraxinus Americana
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2016-01-07
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameFRAXINUS AMERICANA BARK
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0586-3

100 TABLET in 1 CONTAINER (15631-0586-3)
Marketing Start Date2016-01-07
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0586-3 [15631058603]

FRAXINUS AMERICANA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-01-07
Inactivation Date2020-01-31

NDC 15631-0586-7 [15631058607]

FRAXINUS AMERICANA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-01-07
Inactivation Date2020-01-31

NDC 15631-0586-0 [15631058600]

FRAXINUS AMERICANA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-01-07
Inactivation Date2020-01-31

NDC 15631-0586-1 [15631058601]

FRAXINUS AMERICANA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-01-07
Inactivation Date2020-01-31

NDC 15631-0586-5 [15631058605]

FRAXINUS AMERICANA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-01-07
Inactivation Date2020-01-31

NDC 15631-0586-4 [15631058604]

FRAXINUS AMERICANA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-01-07
Inactivation Date2020-01-31

NDC 15631-0586-6 [15631058606]

FRAXINUS AMERICANA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-01-07
Inactivation Date2020-01-31

NDC 15631-0586-2 [15631058602]

FRAXINUS AMERICANA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-01-07
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
FRAXINUS AMERICANA BARK1 [hp_X]/1

OpenFDA Data

SPL SET ID:1eb704ca-62ed-411b-9880-dd0b3fe8d262
Manufacturer
UNII
UPC Code
  • 8907460005526
  • NDC Crossover Matching brand name "FRAXINUS AMERICANA" or generic name "Fraxinus Americana"

    NDCBrand NameGeneric Name
    0220-2155Fraxinus americanaFRAXINUS AMERICANA BARK
    0220-2156Fraxinus americanaFRAXINUS AMERICANA BARK
    15631-0198FRAXINUS AMERICANAFRAXINUS AMERICANA
    15631-0586FRAXINUS AMERICANAFRAXINUS AMERICANA
    68428-394Fraxinus americanaFRAXINUS AMERICANA BARK
    71919-303Fraxinus americanaFRAXINUS AMERICANA BARK
    22840-1425White Ash PollenFraxinus americana
    22840-1426White Ash PollenFraxinus americana
    22840-1427White Ash PollenFraxinus americana
    22840-1428White Ash PollenFraxinus americana
    22840-4430White Ash PollenFraxinus americana
    22840-5407White Ash PollenFraxinus americana
    49643-357White Ash PollenFraxinus americana

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