zinc

Generic: zinc chloride

Labeler: hospira, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name zinc
Generic Name zinc chloride
Labeler hospira, inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

zinc chloride 1 mg/mL

Manufacturer
Hospira, Inc.

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 04094090
Hyphenated Format 0409-4090

Supplemental Identifiers

RxCUI
237508
UNII
86Q357L16B

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 (source: ndc)
Generic Name zinc chloride (source: ndc)
Application Number NDA018959 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 1 mg/mL
source: ndc
Packaging
  • 25 VIAL, PLASTIC in 1 TRAY (0409-4090-01) / 10 mL in 1 VIAL, PLASTIC (0409-4090-11)
source: ndc

Packages (1)

Ingredients (1)

zinc chloride (1 mg/mL)

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"}