Cupric Chloride
- Product NDC
- 70069-506
- 11-digit product format
- 700690506
- Labeler code
- 70069
- Product ID
- 70069-506_ea32e1b7-7c91-478e-9a8c-85f035431e19
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cupric Chloride
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Somerset Therapeutics, LLC
- Application
- ANDA216113
- Marketing category
- ANDA
- Marketing start
- 2024-05-14
- Substance
- CUPRIC CHLORIDE
- Active strength
- .4 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Cupric Chloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CUPRIC CHLORIDE | .4 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | S2QG84156O |
| Rxcui | 204536 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70069-506-01 | Cupric Chloride | 10 mL in 1 VIAL, PLASTIC | INJECTION | 10 | | 4 |
| 70069-506-25 | Cupric Chloride | 25 in 1 CARTON | INJECTION | 25 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70069-506 | CUPRIC CHLORIDE INJECTION [SOMERSET THERAPEUTICS, LLC] | 4 | Current NDC, 2 package rows | 20240514_361d30f2-3c97-4a6c-b252-7fa864d0a625.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70069-506-01 | 70069050601 | 10 mL in 1 VIAL, PLASTIC | 10 ml | | | | Historical |
| 70069-506-25 | 70069050625 | 25 VIAL, PLASTIC in 1 CARTON (70069-506-25) / 10 mL in 1 VIAL, PLASTIC (70069-506-01) | | 2024-05-14 | No | No | Current |