ZINC SULFATE
- Product NDC
- 31722-453
- 11-digit product format
- 317220453
- Labeler code
- 31722
- Product ID
- 31722-453_4c2fa3c5-612d-9133-e063-6394a90ab707
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ZINC SULFATE
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Camber Pharmaceuticals, Inc.
- Application
- ANDA219585
- Marketing category
- ANDA
- Marketing start
- 2025-05-01
- Substance
- ZINC SULFATE
- Active strength
- 1 mg/mL
- Pharmacologic classes
- Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- ZINC SULFATE
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ZINC SULFATE | 1 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 89DS0H96TB |
| Rxcui | 2201521, 2201524, 2369390 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 31722-453-10 | ZINC SULFATE | 10 mL in 1 VIAL | INJECTION, SOLUTION | 10 | | 2 |
| 31722-453-31 | ZINC SULFATE | 25 in 1 CARTON | 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 |
|---|
| 31722-453-10 | 31722045310 | 10 mL in 1 VIAL | 10 ml | | | | Historical |
| 31722-453-31 | 31722045331 | 25 VIAL in 1 CARTON (31722-453-31) / 10 mL in 1 VIAL (31722-453-10) | 25 vial | 2025-05-01 | No | No | Historical |