NDC 15631-0544

CACTUS GRANDIFLORUS

Cactus Grandiflorus

CACTUS GRANDIFLORUS is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Rxhomeo Private Limited D.b.a. Rxhomeo, Inc. The primary component is Selenicereus Grandiflorus Stem.

Product ID15631-0544_4838607d-dc1f-4efa-8907-c84f887a1951
NDC15631-0544
Product TypeHuman Otc Drug
Proprietary NameCACTUS GRANDIFLORUS
Generic NameCactus Grandiflorus
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2015-12-30
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameSELENICEREUS GRANDIFLORUS STEM
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0544-5

500 TABLET in 1 CONTAINER (15631-0544-5)
Marketing Start Date2015-12-30
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0544-1 [15631054401]

CACTUS GRANDIFLORUS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0544-0 [15631054400]

CACTUS GRANDIFLORUS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0544-4 [15631054404]

CACTUS GRANDIFLORUS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0544-7 [15631054407]

CACTUS GRANDIFLORUS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0544-5 [15631054405]

CACTUS GRANDIFLORUS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0544-6 [15631054406]

CACTUS GRANDIFLORUS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0544-2 [15631054402]

CACTUS GRANDIFLORUS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0544-3 [15631054403]

CACTUS GRANDIFLORUS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
SELENICEREUS GRANDIFLORUS STEM3 [hp_X]/1

OpenFDA Data

SPL SET ID:50f15af2-10d2-4883-ae2c-35c115e00e4a
Manufacturer
UNII
UPC Code
  • 8907460005526
  • NDC Crossover Matching brand name "CACTUS GRANDIFLORUS" or generic name "Cactus Grandiflorus"

    NDCBrand NameGeneric Name
    15631-0088CACTUS GRANDIFLORUSCACTUS GRANDIFLORUS
    15631-0544CACTUS GRANDIFLORUSCACTUS GRANDIFLORUS
    60512-6558CACTUS GRANDIFLORUSCACTUS GRANDIFLORUS
    62106-7543CACTUS GRANDIFLORUSNight-blooming Cereus
    63545-558Cactus GrandiflorusCactus Grandiflorus
    63545-559Cactus GrandiflorusCactus Grandiflorus
    63545-560Cactus GrandiflorusCactus Grandiflorus
    63545-561Cactus GrandiflorusCactus Grandiflorus
    63545-562Cactus GrandiflorusCactus Grandiflorus
    63545-563Cactus GrandiflorusCactus Grandiflorus
    63545-564Cactus GrandiflorusCactus Grandiflorus
    63545-565Cactus GrandiflorusCactus Grandiflorus
    63545-566Cactus GrandiflorusCactus Grandiflorus
    68428-267Cactus grandiflorusSELENICEREUS GRANDIFLORUS STEM
    71919-135Cactus grandiflorusSELENICEREUS GRANDIFLORUS STEM
    79718-1137Cactus GrandiflorusCactus Grandiflorus
    69152-1022Cactus grandiflorus 200CCactus grandiflorus
    69152-1099Cactus grandiflorus 30CCactus grandiflorus

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