NDC 15631-0183

EUPATORIUM PURPUREUM

Eupatorium Purpureum

EUPATORIUM PURPUREUM 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 Eutrochium Purpureum Root.

Product ID15631-0183_a11ad69a-19cc-78e9-e053-2a95a90a8b84
NDC15631-0183
Product TypeHuman Otc Drug
Proprietary NameEUPATORIUM PURPUREUM
Generic NameEupatorium Purpureum
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 NameEUTROCHIUM PURPUREUM ROOT
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0183-0

100 PELLET in 1 PACKAGE (15631-0183-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0183-0 [15631018300]

EUPATORIUM PURPUREUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-19

NDC 15631-0183-2 [15631018302]

EUPATORIUM PURPUREUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-19

NDC 15631-0183-1 [15631018301]

EUPATORIUM PURPUREUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-19

NDC 15631-0183-4 [15631018304]

EUPATORIUM PURPUREUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-19

NDC 15631-0183-5 [15631018305]

EUPATORIUM PURPUREUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-19

NDC 15631-0183-3 [15631018303]

EUPATORIUM PURPUREUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-19

Drug Details

Active Ingredients

IngredientStrength
EUTROCHIUM PURPUREUM ROOT1 [hp_X]/1

OpenFDA Data

SPL SET ID:ceb0c608-1873-4881-84cb-6d8575290bc8
Manufacturer
UNII

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

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