NDC 51808-223

Tetrofosmin

Tetrofosmin

Tetrofosmin 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 Tetrofosmin.

• Product ID: 51808-223_0edc9a01-f669-4e7c-af14-cee9bfb3daa3
• NDC: 51808-223
• Product Type: Human Prescription Drug
• Proprietary Name: Tetrofosmin
• Generic Name: Tetrofosmin
• Dosage Form: Injection, Powder, Lyophilized, For Solution
• Route of Administration: INTRAVENOUS
• Marketing Start Date: 2012-05-23
• Marketing Category: UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
• Labeler Name: AnazaoHealth Corporation
• Substance Name: TETROFOSMIN
• Active Ingredient Strength: 0 mg/1
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 51808-223-02

1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 KIT (51808-223-02)

• Marketing Start Date: 2012-05-23
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 51808-223-01 [51808022301]

Tetrofosmin INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

• Marketing Category: Unapproved drug other
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2012-05-23
• Inactivation Date: 2019-11-13

NDC 51808-223-02 [51808022302]

Tetrofosmin INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

• Marketing Category: Unapproved drug other
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2012-05-23
• Inactivation Date: 2019-11-13

Drug Details

Active Ingredients

Ingredient	Strength
TETROFOSMIN	.35 mg/1

OpenFDA Data

• SPL SET ID: 73c67954-938f-4bcc-be48-a5a38094fee3
• Manufacturer:
  • AnazaoHealth Corporation
• UNII:
  • 3J0KPB596Q

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

NDC	Brand Name	Generic Name
51808-223	Tetrofosmin	Tetrofosmin
17156-024	Myoview	Tetrofosmin
17156-026	Myoview	Tetrofosmin