P32 Sodium Phosphate
- Product NDC
- 51808-127
- 11-digit product format
- 518080127
- Labeler code
- 51808
- Product ID
- 51808-127_5ed86373-1e27-42fc-a3b3-b198944f0dff
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- P32 Sodium Phosphate
- Dosage form
- INJECTION, SUSPENSION
- Route
- INTERSTITIAL; INTRA-ARTICULAR; INTRAPERITONEAL; INTRAPLEURAL
- Labeler
- AnazaoHealth Corporation
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2012-06-19
- Marketing end
- 0000-00-00
- Substance
- PHOSPHORUS P-32
- Active strength
- 5 mCi/mL
- 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 |
|---|
| 51808-127-01 | P32 Sodium Phosphate | 3 mL in 1 VIAL | INJECTION, SUSPENSION | 3 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51808-127 | P32 SODIUM PHOSPHATE INJECTION, SUSPENSION [ANAZAOHEALTH CORPORATION] | 1 | Legacy NDC, 1 package rows | 20121015_4996cd1e-4338-43d7-b7aa-418909ab8c16.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 51808-127-01 | 51808012701 | 3 mL in 1 VIAL | 3 ml | Historical |