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
- 60505-6261_c78f555b-3f22-d031-b241-769f29b4c936
- Product NDC
- 60505-6261
- Form
- INJECTION
- Composition / generic term
- Zinc Sulfate Injection
- Labeler
- Apotex Corp
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250115
- Source listing expiry
- 20261231
Source-listed ingredients
- ZINC SULFATE, UNSPECIFIED FORM — 1 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 25 VIAL in 1 CARTON (60505-6261-5) / 10 mL in 1 VIAL (60505-6261-0) · 60505-6261-5
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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