NDC 15631-0695

TARENTULA HISPANA

Tarentula Hispana

TARENTULA HISPANA 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 Lycosa Tarantula.

Product ID15631-0695_c8053ba5-3348-49fe-b9af-d0a1c51ae823
NDC15631-0695
Product TypeHuman Otc Drug
Proprietary NameTARENTULA HISPANA
Generic NameTarentula Hispana
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2015-12-27
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameLYCOSA TARANTULA
Active Ingredient Strength8 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0695-6

1000 TABLET in 1 CONTAINER (15631-0695-6)
Marketing Start Date2015-12-27
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0695-4 [15631069504]

TARENTULA HISPANA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0695-1 [15631069501]

TARENTULA HISPANA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0695-2 [15631069502]

TARENTULA HISPANA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0695-3 [15631069503]

TARENTULA HISPANA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0695-0 [15631069500]

TARENTULA HISPANA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0695-6 [15631069506]

TARENTULA HISPANA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0695-5 [15631069505]

TARENTULA HISPANA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0695-7 [15631069507]

TARENTULA HISPANA TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
LYCOSA TARANTULA8 [hp_X]/1

OpenFDA Data

SPL SET ID:8fb77a40-2d82-4504-8f56-a23cb76105f4
Manufacturer
UNII
UPC Code
  • 8907460005526
  • NDC Crossover Matching brand name "TARENTULA HISPANA" or generic name "Tarentula Hispana"

    NDCBrand NameGeneric Name
    0220-4930Tarentula hispanaLYCOSA TARANTULA
    0220-4931Tarentula hispanaLYCOSA TARANTULA
    0220-4935Tarentula hispanaLYCOSA TARANTULA
    0220-4941Tarentula hispanaLYCOSA TARANTULA
    0220-4942Tarentula hispanaLYCOSA TARANTULA
    0220-4943Tarentula hispanaLYCOSA TARANTULA
    15631-0431TARENTULA HISPANATARENTULA HISPANA
    15631-0695TARENTULA HISPANATARENTULA HISPANA
    62106-6701TARENTULA HISPANATarantula
    68428-665Tarentula hispanaLYCOSA TARANTULA
    71919-664TARENTULA HISPANALycosa tarantula

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.