zinc sulfate
Generic: zinc sulfate
Labeler: gland pharma limitedDrug Facts
Product Profile
Brand Name
zinc sulfate
Generic Name
zinc sulfate
Labeler
gland pharma limited
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
zinc sulfate 1 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
68083-608
Product ID
68083-608_cfa59996-1de2-4313-a7ac-1766764513e2
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA216249
Listing Expiration
2026-12-31
Marketing Start
2023-09-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68083608
Hyphenated Format
68083-608
Supplemental Identifiers
RxCUI
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
ANDA216249 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/mL
Packaging
- 25 VIAL in 1 CARTON (68083-608-25) / 10 mL in 1 VIAL
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "cfa59996-1de2-4313-a7ac-1766764513e2", "openfda": {"unii": ["89DS0H96TB"], "rxcui": ["2201521", "2201524", "2369390"], "spl_set_id": ["8f354f0a-4e10-4e4e-b86c-49d97cbd631d"], "manufacturer_name": ["Gland Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (68083-608-25) / 10 mL in 1 VIAL", "package_ndc": "68083-608-25", "marketing_start_date": "20230901"}], "brand_name": "Zinc Sulfate", "product_id": "68083-608_cfa59996-1de2-4313-a7ac-1766764513e2", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "68083-608", "generic_name": "Zinc Sulfate", "labeler_name": "Gland Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zinc Sulfate", "active_ingredients": [{"name": "ZINC SULFATE", "strength": "1 mg/mL"}], "application_number": "ANDA216249", "marketing_category": "ANDA", "marketing_start_date": "20230901", "listing_expiration_date": "20261231"}