NDC 15631-0034

ANAGALLIS ARVENSIS

Anagallis Arvensis

ANAGALLIS ARVENSIS 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 Anagallis Arvensis.

Product ID15631-0034_90eb495f-cdca-4ac5-a2ca-9d48dd9c3fda
NDC15631-0034
Product TypeHuman Otc Drug
Proprietary NameANAGALLIS ARVENSIS
Generic NameAnagallis Arvensis
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-09-06
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameANAGALLIS ARVENSIS
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0034-0

100 PELLET in 1 PACKAGE (15631-0034-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0034-2 [15631003402]

ANAGALLIS ARVENSIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-10

NDC 15631-0034-5 [15631003405]

ANAGALLIS ARVENSIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-10

NDC 15631-0034-3 [15631003403]

ANAGALLIS ARVENSIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-10

NDC 15631-0034-4 [15631003404]

ANAGALLIS ARVENSIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-10

NDC 15631-0034-1 [15631003401]

ANAGALLIS ARVENSIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-10

NDC 15631-0034-0 [15631003400]

ANAGALLIS ARVENSIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-10

Drug Details

Active Ingredients

IngredientStrength
ANAGALLIS ARVENSIS1 [hp_X]/1

OpenFDA Data

SPL SET ID:9820dfbd-f5ff-461b-b0b4-9460988c9493
Manufacturer
UNII

NDC Crossover Matching brand name "ANAGALLIS ARVENSIS" or generic name "Anagallis Arvensis"

NDCBrand NameGeneric Name
0220-0312Anagallis arvensisANAGALLIS ARVENSIS
15631-0034ANAGALLIS ARVENSISANAGALLIS ARVENSIS
53645-2050Anagallis ArvensisAnagallis Arvensis
53645-2051Anagallis ArvensisAnagallis Arvensis
63545-980Anagallis ArvensisAnagallis Arvernsis
63545-981Anagallis ArvensisAnagallis Arvernsis
63545-982Anagallis ArvensisAnagallis Arvernsis
63545-983Anagallis ArvensisAnagallis Arvernsis
63545-984Anagallis ArvensisAnagallis Arvernsis
63545-985Anagallis ArvensisAnagallis Arvernsis
68428-882Anagallis arvensisANAGALLIS ARVENSIS
71919-054Anagallis arvensisDIAMOND

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