zinc sulfate
- Product NDC
- 70771-1850
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- zinc sulfate
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Zydus Lifesciences Limited
- Application
- ANDA217074
- Marketing category
- ANDA
- Substance
- ZINC SULFATE
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 70771-1850-7 | 25 VIAL in 1 CARTON (70771-1850-7) / 5 mL in 1 VIAL (70771-1850-1) | 2023-12-07 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| ZINC SULFATE INJECTION for intravenous use | Zydus Lifesciences Limited | 2023-08-31 | HUMAN PRESCRIPTION DRUG LABEL | 1 |