NDC 51808-216

Mebrofenin

Mebrofenin

Mebrofenin is a Intravenous Injection, Powder, Lyophilized, For Solution in the Human Prescription Drug category. It is labeled and distributed by Anazaohealth Corporation. The primary component is Mebrofenin.

• Product ID: 51808-216_4d7406b4-8bcd-40f0-a31f-975f5b811da7
• NDC: 51808-216
• Product Type: Human Prescription Drug
• Proprietary Name: Mebrofenin
• Generic Name: Mebrofenin
• Dosage Form: Injection, Powder, Lyophilized, For Solution
• Route of Administration: INTRAVENOUS
• Marketing Start Date: 2012-06-19
• Marketing Category: UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
• Labeler Name: AnazaoHealth Corporation
• Substance Name: MEBROFENIN
• Active Ingredient Strength: 10 mg/1
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 51808-216-01

1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 KIT (51808-216-01)

• Marketing Start Date: 2012-06-19
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 51808-216-01 [51808021601]

Mebrofenin INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

• Marketing Category: Unapproved drug other
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2012-06-19
• Inactivation Date: 2019-11-13

Drug Details

Active Ingredients

Ingredient	Strength
MEBROFENIN	10 mg/1

OpenFDA Data

• SPL SET ID: aeefa6ee-f45c-49fe-b38e-6cfd99a33030
• Manufacturer:
  • AnazaoHealth Corporation
• UNII:
  • 7PV0B6ED98

NDC Crossover Matching brand name "Mebrofenin" or generic name "Mebrofenin"

NDC	Brand Name	Generic Name
51808-216	Mebrofenin	Mebrofenin
0270-0083	Choletec	Mebrofenin