cupric chloride
Generic: cupric chloride
Labeler: amneal pharmaceuticals private limitedDrug Facts
Product Profile
Brand Name
cupric chloride
Generic Name
cupric chloride
Labeler
amneal pharmaceuticals private limited
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
cupric chloride .4 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
80830-2301
Product ID
80830-2301_0483ece7-d1e5-4787-a73e-1b41c75f26a7
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA217287
Listing Expiration
2027-12-31
Marketing Start
2026-01-29
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
808302301
Hyphenated Format
80830-2301
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
cupric chloride (source: ndc)
Generic Name
cupric chloride (source: ndc)
Application Number
ANDA217287 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .4 mg/mL
Packaging
- 25 VIAL in 1 CARTON (80830-2301-5) / 10 mL in 1 VIAL (80830-2301-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "0483ece7-d1e5-4787-a73e-1b41c75f26a7", "openfda": {"unii": ["S2QG84156O"], "rxcui": ["204536"], "spl_set_id": ["c431cc76-f9ba-43c7-8d66-e93c77fa6229"], "manufacturer_name": ["Amneal Pharmaceuticals Private Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (80830-2301-5) / 10 mL in 1 VIAL (80830-2301-1)", "package_ndc": "80830-2301-5", "marketing_start_date": "20260129"}], "brand_name": "CUPRIC CHLORIDE", "product_id": "80830-2301_0483ece7-d1e5-4787-a73e-1b41c75f26a7", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "80830-2301", "generic_name": "CUPRIC CHLORIDE", "labeler_name": "Amneal Pharmaceuticals Private Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CUPRIC CHLORIDE", "active_ingredients": [{"name": "CUPRIC CHLORIDE", "strength": ".4 mg/mL"}], "application_number": "ANDA217287", "marketing_category": "ANDA", "marketing_start_date": "20260129", "listing_expiration_date": "20271231"}