In-111 DTPA
- Product NDC
- 51808-125
- 11-digit product format
- 518080125
- Labeler code
- 51808
- Product ID
- 51808-125_0e714ae6-396c-4488-868e-bfe5fd446f3f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- In-111 DTPA
- Dosage form
- SOLUTION
- Route
- INTRATHECAL
- Labeler
- AnazaoHealth Corporation
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2012-06-19
- Marketing end
- 0000-00-00
- Substance
- INDIUM IN-111 PENTETATE DISODIUM
- Active strength
- 4 mCi/1.5mL
- Pharmacologic classes
- Lead Chelating Activity [MoA],Lead Chelator [EPC]
- 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 |
|---|
| 51808-125-01 | In-111 DTPA | 1.5 mL in 1 VIAL | SOLUTION | 1.5 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51808-125 | IN-111 DTPA SOLUTION [ANAZAOHEALTH CORPORATION] | 1 | Legacy NDC, 1 package rows | 20120709_aa3bd304-ff60-48a1-8576-be99de02e5f6.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 51808-125-01 | 51808012501 | 1.5 mL in 1 VIAL | 1.5 ml | Historical |