NDC 48142-400

Crotoxin

Crotalus Durissus Terrificus Venom

Crotoxin is a Intravenous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Celtic Biotech Iowa, Inc.. The primary component is Crotalus Durissus Terrificus Venom.

• Product ID: 48142-400_8ac1e6de-a534-4abd-8067-b90ce952e8fe
• NDC: 48142-400
• Product Type: Human Prescription Drug
• Proprietary Name: Crotoxin
• Generic Name: Crotalus Durissus Terrificus Venom
• Dosage Form: Injection, Solution
• Route of Administration: INTRAVENOUS
• Marketing Start Date: 2018-04-30
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Celtic Biotech Iowa, Inc.
• Substance Name: CROTALUS DURISSUS TERRIFICUS VENOM
• Active Ingredient Strength: 4 [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 48142-400-40

10 mL in 1 VIAL, MULTI-DOSE (48142-400-40)

• Marketing Start Date: 2018-04-30
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 48142-400-40 [48142040040]

Crotoxin INJECTION, SOLUTION

• Marketing Category: Unapproved homeopathic
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2018-04-30
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
CROTALUS DURISSUS TERRIFICUS VENOM	4 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 148af88b-e23c-4493-9b7f-35d993c32d32
• Manufacturer:
  • Celtic Biotech Iowa, Inc.
• UNII:
  • 2XF6I0446G

NDC Crossover Matching brand name "Crotoxin" or generic name "Crotalus Durissus Terrificus Venom"

NDC	Brand Name	Generic Name
48142-400	Crotoxin	crotalus durissus terrificus venom
0220-1573	Crotalus cascavella	CROTALUS DURISSUS TERRIFICUS VENOM
68428-924	Crotalus cascavella	CROTALUS DURISSUS TERRIFICUS VENOM
71919-234	Crotalus cascavella	CROTALUS DURISSUS TERRIFICUS VENOM