zinc sulfate

Generic: zinc sulfate injection

Labeler: apotex corp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name zinc sulfate
Generic Name zinc sulfate injection
Labeler apotex corp
Dosage Form INJECTION
Routes
INTRAVENOUS
Active Ingredients

zinc sulfate, unspecified form 1 mg/mL

Manufacturer
Apotex Corp

Identifiers & Regulatory

Product NDC 60505-6261
Product ID 60505-6261_c78f555b-3f22-d031-b241-769f29b4c936
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA218059
Listing Expiration 2026-12-31
Marketing Start 2025-01-15

Pharmacologic Class

Classes
copper absorption inhibitor [epc] decreased copper ion absorption [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 605056261
Hyphenated Format 60505-6261

Supplemental Identifiers

RxCUI
2201524 2369390
UNII
89DS0H96TB

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name zinc sulfate (source: ndc)
Generic Name zinc sulfate injection (source: ndc)
Application Number ANDA218059 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 1 mg/mL
source: ndc
Packaging
  • 25 VIAL in 1 CARTON (60505-6261-5) / 10 mL in 1 VIAL (60505-6261-0)
source: ndc

Packages (1)

60505-6261-5 25 VIAL in 1 CARTON (60505-6261-5) / 10 mL in 1 VIAL (60505-6261-0)

Ingredients (1)

zinc sulfate, unspecified form (1 mg/mL)

Linked Drug Pages (1)

Zinc Sulfate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "c78f555b-3f22-d031-b241-769f29b4c936", "openfda": {"unii": ["89DS0H96TB"], "rxcui": ["2201524", "2369390"], "spl_set_id": ["b9cf2dab-6ec8-e099-464a-af46a3601971"], "manufacturer_name": ["Apotex Corp"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (60505-6261-5)  / 10 mL in 1 VIAL (60505-6261-0)", "package_ndc": "60505-6261-5", "marketing_start_date": "20250115"}], "brand_name": "Zinc Sulfate", "product_id": "60505-6261_c78f555b-3f22-d031-b241-769f29b4c936", "dosage_form": "INJECTION", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "60505-6261", "generic_name": "Zinc Sulfate Injection", "labeler_name": "Apotex Corp", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zinc Sulfate", "active_ingredients": [{"name": "ZINC SULFATE, UNSPECIFIED FORM", "strength": "1 mg/mL"}], "application_number": "ANDA218059", "marketing_category": "ANDA", "marketing_start_date": "20250115", "listing_expiration_date": "20261231"}