zinc sulfate

Generic: zinc sulfate injection,

Labeler: zydus pharmaceuticals usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name zinc sulfate
Generic Name zinc sulfate injection,
Labeler zydus pharmaceuticals usa inc.
Dosage Form SOLUTION
Routes
INTRAVENOUS
Active Ingredients

zinc sulfate 3 mg/mL

Manufacturer
Zydus Pharmaceuticals USA Inc.

Identifiers & Regulatory

Product NDC 70710-1877
Product ID 70710-1877_245bc553-262e-47ff-91d0-0b7c136b6413
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217074
Listing Expiration 2026-12-31
Marketing Start 2023-12-07

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 707101877
Hyphenated Format 70710-1877

Supplemental Identifiers

RxCUI
2201521 2201524 2369390
UPC
0370710187675
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 ANDA217074 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 3 mg/mL
source: ndc
Packaging
  • 25 VIAL in 1 CARTON (70710-1877-7) / 10 mL in 1 VIAL (70710-1877-1)
source: ndc

Packages (1)

70710-1877-7 25 VIAL in 1 CARTON (70710-1877-7) / 10 mL in 1 VIAL (70710-1877-1)

Ingredients (1)

zinc sulfate (3 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": "245bc553-262e-47ff-91d0-0b7c136b6413", "openfda": {"upc": ["0370710187675"], "unii": ["89DS0H96TB"], "rxcui": ["2201521", "2201524", "2369390"], "spl_set_id": ["95aa8437-10bc-4205-939f-d21d8fa52a00"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (70710-1877-7)  / 10 mL in 1 VIAL (70710-1877-1)", "package_ndc": "70710-1877-7", "marketing_start_date": "20231207"}], "brand_name": "zinc sulfate", "product_id": "70710-1877_245bc553-262e-47ff-91d0-0b7c136b6413", "dosage_form": "SOLUTION", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "70710-1877", "generic_name": "zinc sulfate injection,", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "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"}