NDC 15631-0580

EUPATORIUM PURPUREUM

Eupatorium Purpureum

EUPATORIUM PURPUREUM 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 Eutrochium Purpureum Root.

Product ID15631-0580_2b649dc0-5bc1-4346-ad44-f7e4101f4219
NDC15631-0580
Product TypeHuman Otc Drug
Proprietary NameEUPATORIUM PURPUREUM
Generic NameEupatorium Purpureum
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2015-12-27
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameEUTROCHIUM PURPUREUM ROOT
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0580-7

10000 TABLET in 1 CONTAINER (15631-0580-7)
Marketing Start Date2015-12-27
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0580-1 [15631058001]

EUPATORIUM PURPUREUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0580-7 [15631058007]

EUPATORIUM PURPUREUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0580-0 [15631058000]

EUPATORIUM PURPUREUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0580-5 [15631058005]

EUPATORIUM PURPUREUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0580-4 [15631058004]

EUPATORIUM PURPUREUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0580-2 [15631058002]

EUPATORIUM PURPUREUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0580-6 [15631058006]

EUPATORIUM PURPUREUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0580-3 [15631058003]

EUPATORIUM PURPUREUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
EUTROCHIUM PURPUREUM ROOT1 [hp_X]/1

OpenFDA Data

SPL SET ID:d2d7dbda-d444-4fb4-b869-09caf351706a
Manufacturer
UNII
UPC Code
  • 8907460005526
  • NDC Crossover Matching brand name "EUPATORIUM PURPUREUM" or generic name "Eupatorium Purpureum"

    NDCBrand NameGeneric Name
    15631-0183EUPATORIUM PURPUREUMEUPATORIUM PURPUREUM
    15631-0580EUPATORIUM PURPUREUMEUPATORIUM PURPUREUM
    71919-279Eupatorium purpureumEUTROCHIUM PURPUREUM ROOT

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