NDC 15631-0159

CROTALUS HORRIDUS

Crotalus Horridus

CROTALUS HORRIDUS 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 Crotalus Horridus Horridus Venom.

Product ID15631-0159_07bae010-0fb6-44fe-9bcb-604f5c256945
NDC15631-0159
Product TypeHuman Otc Drug
Proprietary NameCROTALUS HORRIDUS
Generic NameCrotalus Horridus
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-10-02
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameCROTALUS HORRIDUS HORRIDUS VENOM
Active Ingredient Strength8 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0159-0

100 PELLET in 1 PACKAGE (15631-0159-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0159-3 [15631015903]

CROTALUS HORRIDUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-17

NDC 15631-0159-1 [15631015901]

CROTALUS HORRIDUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-17

NDC 15631-0159-2 [15631015902]

CROTALUS HORRIDUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-17

NDC 15631-0159-4 [15631015904]

CROTALUS HORRIDUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-17

NDC 15631-0159-5 [15631015905]

CROTALUS HORRIDUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-17

NDC 15631-0159-0 [15631015900]

CROTALUS HORRIDUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-17

Drug Details

Active Ingredients

IngredientStrength
CROTALUS HORRIDUS HORRIDUS VENOM8 [hp_X]/1

OpenFDA Data

SPL SET ID:21fe689d-f4fb-416f-93f6-218e62bc26f0
Manufacturer
UNII

NDC Crossover Matching brand name "CROTALUS HORRIDUS" or generic name "Crotalus Horridus"

NDCBrand NameGeneric Name
0220-1577Crotalus horridusCROTALUS HORRIDUS HORRIDUS VENOM
0220-1578Crotalus horridusCROTALUS HORRIDUS HORRIDUS VENOM
0220-1579Crotalus horridusCROTALUS HORRIDUS HORRIDUS VENOM
15631-0159CROTALUS HORRIDUSCROTALUS HORRIDUS
62106-6619CROTALUS HORRIDUSTimber rattlesnake
66096-825Crotalus HorridusCROTALUS HORRIDUS
68428-345Crotalus horridusCROTALUS HORRIDUS HORRIDUS VENOM
71919-235CROTALUS HORRIDUSCrotalus horridus horridus venom
69152-1106Crotalus horridus 200CCrotalus horridus
43742-0513EBOLA REMEDYCrotalus Horridus

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