NDC 51808-128

P32 Sodium Phosphate

P32 Sodium Phosphate

P32 Sodium Phosphate is a Intravenous Solution in the Human Prescription Drug category. It is labeled and distributed by Anazaohealth Corporation. The primary component is Phosphorus P-32.

• Product ID: 51808-128_c099d1ae-d9f6-4176-b55c-233ce52b2976
• NDC: 51808-128
• Product Type: Human Prescription Drug
• Proprietary Name: P32 Sodium Phosphate
• Generic Name: P32 Sodium Phosphate
• 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: PHOSPHORUS P-32
• Active Ingredient Strength: 10 mCi/4mL
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 51808-128-01

4 mL in 1 VIAL (51808-128-01)

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

NDC SPL Data Element Entries

NDC 51808-128-01 [51808012801]

P32 Sodium Phosphate SOLUTION

• Marketing Category: Unapproved drug other
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2012-06-19
• Inactivation Date: 2019-11-27

Drug Details

Active Ingredients

Ingredient	Strength
PHOSPHORUS P-32	10 mCi/4mL

OpenFDA Data

• SPL SET ID: 735f92e3-cc92-4d9b-afe8-f935a685ee78
• Manufacturer:
  • AnazaoHealth Corporation
• UNII:
  • 690284A407

NDC Crossover Matching brand name "P32 Sodium Phosphate" or generic name "P32 Sodium Phosphate"

NDC	Brand Name	Generic Name
51808-127	P32 Sodium Phosphate	P32 Sodium Phosphate
51808-128	P32 Sodium Phosphate	P32 Sodium Phosphate