cupric chloride

Generic: cupric chloride

Labeler: amneal pharmaceuticals private limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cupric chloride
Generic Name cupric chloride
Labeler amneal pharmaceuticals private limited
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

cupric chloride .4 mg/mL

Manufacturer
Amneal Pharmaceuticals Private Limited

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
204536
UNII
S2QG84156O

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 cupric chloride (source: ndc)
Generic Name cupric chloride (source: ndc)
Application Number ANDA217287 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • .4 mg/mL
source: ndc
Packaging
  • 25 VIAL in 1 CARTON (80830-2301-5) / 10 mL in 1 VIAL (80830-2301-1)
source: ndc

Packages (1)

Ingredients (1)

cupric chloride (.4 mg/mL)

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"}