NDC 15631-0430

TARENTULA CUBENSIS

Tarentula Cubensis

TARENTULA CUBENSIS 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 Citharacanthus Spinicrus.

Product ID15631-0430_196c7db4-de5d-4aba-9d0f-594a3d0f1d0d
NDC15631-0430
Product TypeHuman Otc Drug
Proprietary NameTARENTULA CUBENSIS
Generic NameTarentula Cubensis
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-10-31
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameCITHARACANTHUS SPINICRUS
Active Ingredient Strength8 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0430-0

100 PELLET in 1 VIAL, SINGLE-DOSE (15631-0430-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0430-4 [15631043004]

TARENTULA CUBENSIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0430-5 [15631043005]

TARENTULA CUBENSIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0430-0 [15631043000]

TARENTULA CUBENSIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0430-1 [15631043001]

TARENTULA CUBENSIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0430-3 [15631043003]

TARENTULA CUBENSIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0430-2 [15631043002]

TARENTULA CUBENSIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

Drug Details

Active Ingredients

IngredientStrength
CITHARACANTHUS SPINICRUS8 [hp_X]/1

OpenFDA Data

SPL SET ID:b085e5f1-5160-437a-8004-d35f7d321635
Manufacturer
UNII

NDC Crossover Matching brand name "TARENTULA CUBENSIS" or generic name "Tarentula Cubensis"

NDCBrand NameGeneric Name
0220-4937Tarentula cubensisCITHARACANTHUS SPINICRUS
0220-4938Tarentula cubensisCITHARACANTHUS SPINICRUS
15631-0429TARENTULA CUBENSISTARENTULA CUBENSIS
15631-0430TARENTULA CUBENSISTARENTULA CUBENSIS
68428-664Tarentula cubensisCITHARACANTHUS SPINICRUS
71919-666TARENTULA CUBENSISCitharacanthus spinicrus

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