P32 Sodium Phosphate
- Product NDC
- 51808-128
- 11-digit product format
- 518080128
- Labeler code
- 51808
- Product ID
- 51808-128_c099d1ae-d9f6-4176-b55c-233ce52b2976
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- P32 Sodium Phosphate
- Dosage form
- SOLUTION
- Route
- INTRAVENOUS
- Labeler
- AnazaoHealth Corporation
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2012-06-19
- Marketing end
- 0000-00-00
- Substance
- PHOSPHORUS P-32
- Active strength
- 10 mCi/4mL
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51808-128-01 | P32 Sodium Phosphate | 4 mL in 1 VIAL | SOLUTION | 4 | | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51808-128 | P32 SODIUM PHOSPHATE SOLUTION [ANAZAOHEALTH CORPORATION] | 2 | Legacy NDC, 1 package rows | 20121015_735f92e3-cc92-4d9b-afe8-f935a685ee78.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 51808-128-01 | 51808012801 | 4 mL in 1 VIAL | 4 ml | Historical |