United States · FDA National Drug Code directory
zinc sulfate
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 70710-1878_245bc553-262e-47ff-91d0-0b7c136b6413
- Product NDC
- 70710-1878
- Form
- SOLUTION
- Composition / generic term
- zinc sulfate injection,
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20231207
- Source listing expiry
- 20261231
Source-listed ingredients
- ZINC SULFATE — 5 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 25 VIAL in 1 CARTON (70710-1878-7) / 5 mL in 1 VIAL (70710-1878-1) · 70710-1878-7
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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