NDC 51808-101

Sodium Chromate 51

Sodium Chromate 51

Sodium Chromate 51 is a Intravenous Solution in the Human Prescription Drug category. It is labeled and distributed by Anazaohealth Corporation. The primary component is Chromium Cr-51.

• Product ID: 51808-101_40ecc37d-84df-4f1c-ab4b-30d0c06718a2
• NDC: 51808-101
• Product Type: Human Prescription Drug
• Proprietary Name: Sodium Chromate 51
• Generic Name: Sodium Chromate 51
• Dosage Form: 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: CHROMIUM CR-51
• Active Ingredient Strength: 1 mCi/5mL
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 51808-101-02

5 mL in 1 VIAL (51808-101-02)

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

NDC SPL Data Element Entries

NDC 51808-101-01 [51808010101]

Sodium Chromate 51 SOLUTION

• Marketing Category: Unapproved drug other
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2012-06-19
• Marketing End Date: 2012-10-23

NDC 51808-101-02 [51808010102]

Sodium Chromate 51 SOLUTION

• Marketing Category: Unapproved drug other
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2012-10-23
• Inactivation Date: 2019-11-27

Drug Details

Active Ingredients

Ingredient	Strength
CHROMIUM CR-51	1 mCi/5mL

OpenFDA Data

• SPL SET ID: 0cc2c204-c14d-456b-b630-9e50d683a937
• Manufacturer:
  • AnazaoHealth Corporation
• UNII:
  • 9QAU17N705