Zinc sulfate
- Product NDC
- 70069-692
- 11-digit product format
- 700690692
- Labeler code
- 70069
- Product ID
- 70069-692_e1880316-9556-4529-8ba1-8669113a993e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Zinc sulfate
- Dosage form
- SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Somerset Therapeutics, LLC
- Application
- ANDA216135
- Marketing category
- ANDA
- Marketing start
- 2024-07-18
- Substance
- ZINC SULFATE
- Active strength
- 3 mg/mL
- Pharmacologic classes
- Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Zinc sulfate
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ZINC SULFATE | 3 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 89DS0H96TB |
| Rxcui | 2201521, 2201524 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70069-692-01 | Zinc sulfate | 10 mL in 1 VIAL | SOLUTION | 10 | | 3 |
| 70069-692-25 | Zinc sulfate | 25 in 1 CARTON | SOLUTION | 25 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70069-692 | ZINC SULFATE SOLUTION [SOMERSET THERAPEUTICS, LLC] | 3 | Current NDC, 2 package rows | 20240719_c9d45d0e-a165-4112-81f9-c0e455572ecf.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 |
|---|
| 70069-692-01 | 70069069201 | 10 mL in 1 VIAL | 10 ml | | | | Historical |
| 70069-692-25 | 70069069225 | 25 VIAL in 1 CARTON (70069-692-25) / 10 mL in 1 VIAL (70069-692-01) | 25 vial | 2024-07-18 | No | No | Current |