Sodium Chromate 51
- Product NDC
- 51808-101
- 11-digit product format
- 518080101
- Labeler code
- 51808
- Product ID
- 51808-101_40ecc37d-84df-4f1c-ab4b-30d0c06718a2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Chromate 51
- Dosage form
- SOLUTION
- Route
- INTRAVENOUS
- Labeler
- AnazaoHealth Corporation
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2012-06-19
- Marketing end
- 0000-00-00
- Substance
- CHROMIUM CR-51
- Active strength
- 1 mCi/5mL
- 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 |
|---|
| 51808-101-02 | Sodium Chromate 51 | 5 mL in 1 VIAL | SOLUTION | 5 | | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51808-101 | SODIUM CHROMATE 51 SOLUTION [ANAZAOHEALTH CORPORATION] | 2 | Legacy NDC, 1 package rows | 20121023_0cc2c204-c14d-456b-b630-9e50d683a937.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 51808-101-02 | 51808010102 | 5 mL in 1 VIAL | 5 ml | Historical |