zinc sulfate
- Product NDC
- 70771-1848
- 11-digit product format
- 707711848
- Labeler code
- 70771
- Product ID
- 70771-1848_4a7d1f4a-5a38-48a6-9eae-0616d6c77ecd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- zinc sulfate
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Zydus Lifesciences Limited
- Application
- ANDA217074
- Marketing category
- ANDA
- Marketing start
- 2023-12-07
- 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
- 2026-12-31
- Current FDA listing
- Yes
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70771-1848-7 | 70771184807 | 25 VIAL in 1 CARTON (70771-1848-7) / 10 mL in 1 VIAL (70771-1848-1) | 25 vial | 2023-12-07 | No | No | Historical |