NDC 15631-0013

ALETRIS FARINOSA

Aletris Farinosa

ALETRIS FARINOSA 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 Aletris Farinosa Root.

Product ID15631-0013_2362a532-6489-4779-8356-545c46df75a4
NDC15631-0013
Product TypeHuman Otc Drug
Proprietary NameALETRIS FARINOSA
Generic NameAletris Farinosa
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 NameALETRIS FARINOSA ROOT
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0013-0

100 PELLET in 1 PACKAGE (15631-0013-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0013-3 [15631001303]

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

NDC 15631-0013-5 [15631001305]

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

NDC 15631-0013-2 [15631001302]

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

NDC 15631-0013-0 [15631001300]

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

NDC 15631-0013-4 [15631001304]

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

NDC 15631-0013-1 [15631001301]

ALETRIS FARINOSA 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
ALETRIS FARINOSA ROOT1 [hp_X]/1

OpenFDA Data

SPL SET ID:83b63c7c-9391-4112-b42d-b298fe741f98
Manufacturer
UNII

NDC Crossover Matching brand name "ALETRIS FARINOSA" or generic name "Aletris Farinosa"

NDCBrand NameGeneric Name
0220-0160Aletris farinosaALETRIS FARINOSA ROOT
15631-0013ALETRIS FARINOSAALETRIS FARINOSA
60512-6468ALETRIS FARINOSAALETRIS FARINOSA
68428-187Aletris farinosaALETRIS FARINOSA ROOT
71919-026Aletris farinosaALETRIS FARINOSA ROOT

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