NDC 15631-0184

EUPHRASIA OFFICINALIS

Euphrasia Officinalis

EUPHRASIA OFFICINALIS 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 Euphrasia Stricta.

Product ID15631-0184_78816cd8-9564-4ee6-b7e1-1db249271e2a
NDC15631-0184
Product TypeHuman Otc Drug
Proprietary NameEUPHRASIA OFFICINALIS
Generic NameEuphrasia Officinalis
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 NameEUPHRASIA STRICTA
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0184-0

100 PELLET in 1 PACKAGE (15631-0184-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0184-1 [15631018401]

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

NDC 15631-0184-2 [15631018402]

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

NDC 15631-0184-4 [15631018404]

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

NDC 15631-0184-3 [15631018403]

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

NDC 15631-0184-0 [15631018400]

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

NDC 15631-0184-5 [15631018405]

EUPHRASIA OFFICINALIS 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
EUPHRASIA STRICTA1 [hp_X]/1

OpenFDA Data

SPL SET ID:1cf52c36-a405-40a8-a492-20df572aedf2
Manufacturer
UNII

NDC Crossover Matching brand name "EUPHRASIA OFFICINALIS" or generic name "Euphrasia Officinalis"

NDCBrand NameGeneric Name
0220-1988Euphrasia officinalisEUPHRASIA STRICTA
0220-1989Euphrasia officinalisEUPHRASIA STRICTA
0220-1990Euphrasia officinalisEUPHRASIA STRICTA
0220-1994Euphrasia officinalisEUPHRASIA STRICTA
0220-1995Euphrasia officinalisEUPHRASIA STRICTA
0220-1996Euphrasia officinalisEUPHRASIA STRICTA
0220-1997Euphrasia officinalisEUPHRASIA STRICTA
0220-1998Euphrasia officinalisEUPHRASIA STRICTA
0360-0172EUPHRASIA OFFICINALISEUPHRASIA
15631-0184EUPHRASIA OFFICINALISEUPHRASIA OFFICINALIS
15631-0581EUPHRASIA OFFICINALISEUPHRASIA OFFICINALIS
37662-0825Euphrasia OfficinalisEuphrasia Officinalis
37662-0826Euphrasia OfficinalisEuphrasia Officinalis
37662-0827Euphrasia OfficinalisEuphrasia Officinalis
37662-0828Euphrasia OfficinalisEuphrasia Officinalis
37662-0829Euphrasia OfficinalisEuphrasia Officinalis
37662-0830Euphrasia OfficinalisEuphrasia Officinalis
37662-0831Euphrasia OfficinalisEuphrasia Officinalis
37662-0832Euphrasia OfficinalisEuphrasia Officinalis
37662-0833Euphrasia OfficinalisEuphrasia Officinalis
60512-1018EUPHRASIA OFFICINALISEUPHRASIA OFFICINALIS
62106-8020EUPHRASIA OFFICINALISEuphrasy
63083-7117Euphrasia officinalisEuphrasia officinalis
68428-377Euphrasia officinalisEUPHRASIA STRICTA
71919-282Euphrasia officinalisEUPHRASIA STRICTA
76472-4049EUPHRASIA OFFICINALISEUPHRASIA OFFICINALIS
76472-4081EUPHRASIA OFFICINALISEUPHRASIA OFFICINALIS

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