CHROMIUM CHROMIC CHLORIDE
- Product NDC
- 51662-1415
- 11-digit product format
- 516621415
- Labeler code
- 51662
- Product ID
- 51662-1415_9f33e3f2-3fd3-4fa0-e053-2a95a90aba01
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CHROMIUM CHROMIC CHLORIDE
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- HF Acquisition Co LLC, DBA HealthFirst
- Application
- NDA018961
- Marketing category
- NDA
- Marketing start
- 2019-10-18
- Marketing end
- 0000-00-00
- Substance
- CHROMIC CHLORIDE
- Active strength
- 4 ug/mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 51662-1415-1 | CHROMIUM CHROMIC CHLORIDE | 10 mL in 1 VIAL, PLASTIC | INJECTION, SOLUTION | 10 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51662-1415 | CHROMIUM CHROMIC CHLORIDE INJECTION, SOLUTION [HF ACQUISITION CO LLC, DBA HEALTHFIRST] | 2 | Legacy NDC, 1 package rows | 20200223_953ad6e9-c066-6dc3-e053-2a95a90a9025.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51662-1415-1 | 51662141501 | 10 mL in 1 VIAL, PLASTIC (51662-1415-1) | 10 ml | 2019-10-18 | 0000-00-00 | No | No | Current |