NDC 15631-0322

OPUNTIA VULGARIS

Opuntia Vulgaris

OPUNTIA VULGARIS 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 Opuntia Ficus-indica.

Product ID15631-0322_1e743a99-4a34-4f7f-ab4a-256b7517bd71
NDC15631-0322
Product TypeHuman Otc Drug
Proprietary NameOPUNTIA VULGARIS
Generic NameOpuntia Vulgaris
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-09-10
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameOPUNTIA FICUS-INDICA
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0322-0

100 PELLET in 1 PACKAGE (15631-0322-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0322-3 [15631032203]

OPUNTIA VULGARIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0322-4 [15631032204]

OPUNTIA VULGARIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0322-0 [15631032200]

OPUNTIA VULGARIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0322-1 [15631032201]

OPUNTIA VULGARIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0322-5 [15631032205]

OPUNTIA VULGARIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0322-2 [15631032202]

OPUNTIA VULGARIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

Drug Details

Active Ingredients

IngredientStrength
OPUNTIA FICUS-INDICA1 [hp_X]/1

OpenFDA Data

SPL SET ID:cbfd49a0-8190-4b3b-b07a-057a65d7242d
Manufacturer
UNII

NDC Crossover Matching brand name "OPUNTIA VULGARIS" or generic name "Opuntia Vulgaris"

NDCBrand NameGeneric Name
15631-0322OPUNTIA VULGARISOPUNTIA VULGARIS
68428-544Opuntia vulgarisOPUNTIA FICUS-INDICA
71919-507Opuntia vulgarisOPUNTIA FICUS-INDICA

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