CUPRIC CHLORIDE
- Product NDC
- 84897-013
- 11-digit product format
- 848970013
- Labeler code
- 84897
- Product ID
- 84897-013_7d9f7399-2dfe-4c5a-9946-f011d8a8c6fe
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CUPRIC CHLORIDE
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Renova Pharmaceuticals LLC
- Application
- ANDA217626
- Marketing category
- ANDA
- Marketing start
- 2026-05-07
- Substance
- CUPRIC CHLORIDE
- Active strength
- .4 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- CUPRIC CHLORIDE
- Listing expiration
- 2027-12-31
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 |
|---|
| 84897-013-01 | CUPRIC CHLORIDE | 10 mL in 1 VIAL, SINGLE-DOSE | INJECTION, SOLUTION | 10 | | 2 |
| 84897-013-25 | CUPRIC CHLORIDE | 25 in 1 PACKAGE | INJECTION, SOLUTION | 25 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 84897-013-01 | 84897001301 | 10 mL in 1 VIAL, SINGLE-DOSE | 10 ml | | | | Historical |
| 84897-013-25 | 84897001325 | 25 VIAL, SINGLE-DOSE in 1 PACKAGE (84897-013-25) / 10 mL in 1 VIAL, SINGLE-DOSE (84897-013-01) | | 2026-05-07 | No | No | Historical |