zinc sulfate
Generic: zinc sulfate
Labeler: zydus lifesciences limitedDrug Facts
Product Profile
Brand Name
zinc sulfate
Generic Name
zinc sulfate
Labeler
zydus lifesciences limited
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
zinc sulfate 3 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
70771-1849
Product ID
70771-1849_4a7d1f4a-5a38-48a6-9eae-0616d6c77ecd
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA217074
Listing Expiration
2026-12-31
Marketing Start
2023-12-07
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
707711849
Hyphenated Format
70771-1849
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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 (source: ndc)
Application Number
ANDA217074 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 3 mg/mL
Packaging
- 25 VIAL in 1 CARTON (70771-1849-7) / 10 mL in 1 VIAL (70771-1849-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "4a7d1f4a-5a38-48a6-9eae-0616d6c77ecd", "openfda": {"upc": ["0370710187675"], "unii": ["89DS0H96TB"], "rxcui": ["2201521", "2201524", "2369390"], "spl_set_id": ["74d8d07b-cfd9-4262-b689-fea12673bbd1"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (70771-1849-7) / 10 mL in 1 VIAL (70771-1849-1)", "package_ndc": "70771-1849-7", "marketing_start_date": "20231207"}], "brand_name": "zinc sulfate", "product_id": "70771-1849_4a7d1f4a-5a38-48a6-9eae-0616d6c77ecd", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "70771-1849", "generic_name": "zinc sulfate", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "zinc sulfate", "active_ingredients": [{"name": "ZINC SULFATE", "strength": "3 mg/mL"}], "application_number": "ANDA217074", "marketing_category": "ANDA", "marketing_start_date": "20231207", "listing_expiration_date": "20261231"}