zinc sulfate
Generic: zinc sulfate
Labeler: camber pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
zinc sulfate
Generic Name
zinc sulfate
Labeler
camber pharmaceuticals, inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
zinc sulfate 1 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
31722-453
Product ID
31722-453_4c2fa3c5-612d-9133-e063-6394a90ab707
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA219585
Listing Expiration
2027-12-31
Marketing Start
2025-05-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
31722453
Hyphenated Format
31722-453
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
ANDA219585 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/mL
Packaging
- 25 VIAL in 1 CARTON (31722-453-31) / 10 mL in 1 VIAL (31722-453-10)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "4c2fa3c5-612d-9133-e063-6394a90ab707", "openfda": {"upc": ["0331722453103", "0331722455329", "0331722454100"], "unii": ["89DS0H96TB"], "rxcui": ["2201521", "2201524", "2369390"], "spl_set_id": ["49698d00-f44b-4b1f-ae34-6b9067911757"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (31722-453-31) / 10 mL in 1 VIAL (31722-453-10)", "package_ndc": "31722-453-31", "marketing_start_date": "20250501"}], "brand_name": "ZINC SULFATE", "product_id": "31722-453_4c2fa3c5-612d-9133-e063-6394a90ab707", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "31722-453", "generic_name": "ZINC SULFATE", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ZINC SULFATE", "active_ingredients": [{"name": "ZINC SULFATE", "strength": "1 mg/mL"}], "application_number": "ANDA219585", "marketing_category": "ANDA", "marketing_start_date": "20250501", "listing_expiration_date": "20271231"}