NDC 15631-0511

ANACARDIUM OCCIDENTALE

Anacardium Occidentale

ANACARDIUM OCCIDENTALE 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 Anacardium Occidentale Fruit.

Product ID15631-0511_dc774477-c03d-4fc5-9005-83e557ee8b4c
NDC15631-0511
Product TypeHuman Otc Drug
Proprietary NameANACARDIUM OCCIDENTALE
Generic NameAnacardium Occidentale
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2015-12-07
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameANACARDIUM OCCIDENTALE FRUIT
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0511-7

10000 TABLET in 1 CONTAINER (15631-0511-7)
Marketing Start Date2015-12-07
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0511-4 [15631051104]

ANACARDIUM OCCIDENTALE TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-07
Inactivation Date2020-01-31

NDC 15631-0511-0 [15631051100]

ANACARDIUM OCCIDENTALE TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-07
Inactivation Date2020-01-31

NDC 15631-0511-3 [15631051103]

ANACARDIUM OCCIDENTALE TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-07
Inactivation Date2020-01-31

NDC 15631-0511-5 [15631051105]

ANACARDIUM OCCIDENTALE TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-07
Inactivation Date2020-01-31

NDC 15631-0511-7 [15631051107]

ANACARDIUM OCCIDENTALE TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-07
Inactivation Date2020-01-31

NDC 15631-0511-6 [15631051106]

ANACARDIUM OCCIDENTALE TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-07
Inactivation Date2020-01-31

NDC 15631-0511-2 [15631051102]

ANACARDIUM OCCIDENTALE TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-07
Inactivation Date2020-01-31

NDC 15631-0511-1 [15631051101]

ANACARDIUM OCCIDENTALE TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-07
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
ANACARDIUM OCCIDENTALE FRUIT3 [hp_X]/1

OpenFDA Data

SPL SET ID:a7346aff-28ee-4314-b1f6-d61c3b833ab9
Manufacturer
UNII
UPC Code
  • 8907460005526
  • NDC Crossover Matching brand name "ANACARDIUM OCCIDENTALE" or generic name "Anacardium Occidentale"

    NDCBrand NameGeneric Name
    0220-0304Anacardium occidentaleANACARDIUM OCCIDENTALE FRUIT
    15631-0032ANACARDIUM OCCIDENTALEANACARDIUM OCCIDENTALE
    15631-0511ANACARDIUM OCCIDENTALEANACARDIUM OCCIDENTALE
    63545-962Anacardium OccidentaleAnacardium Occidentale
    63545-963Anacardium OccidentaleAnacardium Occidentale
    63545-964Anacardium OccidentaleAnacardium Occidentale
    63545-965Anacardium OccidentaleAnacardium Occidentale
    63545-966Anacardium OccidentaleAnacardium Occidentale
    63545-967Anacardium OccidentaleAnacardium Occidentale
    63545-968Anacardium OccidentaleAnacardium Occidentale
    63545-969Anacardium OccidentaleAnacardium Occidentale
    63545-970Anacardium OccidentaleAnacardium Occidentale
    68428-203Anacardium occidentaleANACARDIUM OCCIDENTALE FRUIT
    71919-052Anacardium occidentaleANACARDIUM OCCIDENTALE FRUIT
    79718-1014Anacardium OccidentaleAnacardium Occidentale
    79718-1071Anacardium OccidentaleAnacardium Occidentale
    22840-5783Cashew NutAnacardium occidentale

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