zinc
Generic: zinc chloride
Labeler: hospira, inc.Drug Facts
Product Profile
Brand Name
zinc
Generic Name
zinc chloride
Labeler
hospira, inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
zinc chloride 1 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0409-4090
Product ID
0409-4090_24885d38-87ae-4ab3-a7b3-95c55838a8b9
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA018959
Listing Expiration
2026-12-31
Marketing Start
1990-09-30
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
04094090
Hyphenated Format
0409-4090
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 (source: ndc)
Generic Name
zinc chloride (source: ndc)
Application Number
NDA018959 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/mL
Packaging
- 25 VIAL, PLASTIC in 1 TRAY (0409-4090-01) / 10 mL in 1 VIAL, PLASTIC (0409-4090-11)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "24885d38-87ae-4ab3-a7b3-95c55838a8b9", "openfda": {"unii": ["86Q357L16B"], "rxcui": ["237508"], "spl_set_id": ["9a1914a0-e195-4233-c1be-bc2075580eb8"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, PLASTIC in 1 TRAY (0409-4090-01) / 10 mL in 1 VIAL, PLASTIC (0409-4090-11)", "package_ndc": "0409-4090-01", "marketing_start_date": "19900930"}], "brand_name": "ZINC", "product_id": "0409-4090_24885d38-87ae-4ab3-a7b3-95c55838a8b9", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "0409-4090", "generic_name": "ZINC CHLORIDE", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ZINC", "active_ingredients": [{"name": "ZINC CHLORIDE", "strength": "1 mg/mL"}], "application_number": "NDA018959", "marketing_category": "NDA", "marketing_start_date": "19900930", "listing_expiration_date": "20261231"}