NDC 15631-0173

ECHINACEA ANGUSTIFOLIA

Echinacea Angustifolia

ECHINACEA ANGUSTIFOLIA 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 Echinacea Angustifolia.

Product ID15631-0173_1e54508b-e542-4a63-96ba-2f573cb69a70
NDC15631-0173
Product TypeHuman Otc Drug
Proprietary NameECHINACEA ANGUSTIFOLIA
Generic NameEchinacea Angustifolia
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 NameECHINACEA ANGUSTIFOLIA
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0173-0

100 PELLET in 1 PACKAGE (15631-0173-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0173-0 [15631017300]

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

NDC 15631-0173-3 [15631017303]

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

NDC 15631-0173-5 [15631017305]

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

NDC 15631-0173-1 [15631017301]

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

NDC 15631-0173-2 [15631017302]

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

NDC 15631-0173-4 [15631017304]

ECHINACEA ANGUSTIFOLIA 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
ECHINACEA ANGUSTIFOLIA1 [hp_X]/1

OpenFDA Data

SPL SET ID:0d900fc6-b4bc-4de9-9593-b3759ffa95d9
Manufacturer
UNII

NDC Crossover Matching brand name "ECHINACEA ANGUSTIFOLIA" or generic name "Echinacea Angustifolia"

NDCBrand NameGeneric Name
0220-1841Echinacea angustifoliaECHINACEA ANGUSTIFOLIA
0220-1842Echinacea angustifoliaECHINACEA ANGUSTIFOLIA
0220-1843Echinacea angustifoliaECHINACEA ANGUSTIFOLIA
0220-1844Echinacea angustifoliaECHINACEA ANGUSTIFOLIA
0220-1845Echinacea angustifoliaECHINACEA ANGUSTIFOLIA
0220-1846Echinacea angustifoliaECHINACEA ANGUSTIFOLIA
0220-1847Echinacea angustifoliaECHINACEA ANGUSTIFOLIA
0220-1852Echinacea angustifoliaECHINACEA ANGUSTIFOLIA
0360-0162ECHINACEA ANGUSTIFOLIAECHINACEA ANGUST.
0360-0163ECHINACEA ANGUSTIFOLIAECHINACEA ANGUST.
15631-0173ECHINACEA ANGUSTIFOLIAECHINACEA ANGUSTIFOLIA
15631-0577ECHINACEA ANGUSTIFOLIAECHINACEA ANGUSTIFOLIA
37662-0665Echinacea AngustifoliaEchinacea Angustifolia
37662-0666Echinacea AngustifoliaEchinacea Angustifolia
37662-0667Echinacea AngustifoliaEchinacea Angustifolia
37662-0668Echinacea AngustifoliaEchinacea Angustifolia
37662-0669Echinacea AngustifoliaEchinacea Angustifolia
37662-0670Echinacea AngustifoliaEchinacea Angustifolia
37662-0671Echinacea AngustifoliaEchinacea Angustifolia
37662-0672Echinacea AngustifoliaEchinacea Angustifolia
60512-6650ECHINACEA ANGUSTIFOLIAECHINACEA ANGUSTIFOLIA
68428-361Echinacea angustifoliaECHINACEA ANGUSTIFOLIA
71919-262Echinacea angustifoliaECHINACEA ANGUSTIFOLIA
64117-141Carbuncles BoilsECHINACEA ANGUSTIFOLIA
68428-143Echinacea Ang Kit RefillECHINACEA ANGUSTIFOLIA

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