zinc sulfate
- Product NDC
- 70710-1878
- 11-digit product format
- 707101878
- Labeler code
- 70710
- Product ID
- 70710-1878_245bc553-262e-47ff-91d0-0b7c136b6413
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- zinc sulfate injection,
- Dosage form
- SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Application
- ANDA217074
- Marketing category
- ANDA
- Marketing start
- 2023-12-07
- Substance
- ZINC SULFATE
- Active strength
- 5 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
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70710-1878-7 | 70710187807 | 25 VIAL in 1 CARTON (70710-1878-7) / 5 mL in 1 VIAL (70710-1878-1) | 25 vial | 2023-12-07 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| zinc sulfate injection, | Zydus Pharmaceuticals USA Inc. | Zydus Lifesciences Limited | 2024-12-06 | HUMAN PRESCRIPTION DRUG LABEL | 2 |