cupric chloride

Generic: cupric chloride

Labeler: somerset therapeutics, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cupric chloride
Generic Name cupric chloride
Labeler somerset therapeutics, llc
Dosage Form INJECTION
Routes
INTRAVENOUS
Active Ingredients

cupric chloride .4 mg/mL

Manufacturer
Somerset Therapeutics, LLC

Identifiers & Regulatory

Product NDC 70069-506
Product ID 70069-506_ea32e1b7-7c91-478e-9a8c-85f035431e19
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216113
Listing Expiration 2026-12-31
Marketing Start 2024-05-14

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70069506
Hyphenated Format 70069-506

Supplemental Identifiers

RxCUI
204536
UPC
0370069506011
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 ANDA216113 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • .4 mg/mL
source: ndc
Packaging
  • 25 VIAL, PLASTIC in 1 CARTON (70069-506-25) / 10 mL in 1 VIAL, PLASTIC (70069-506-01)
source: ndc

Packages (1)

70069-506-25 25 VIAL, PLASTIC in 1 CARTON (70069-506-25) / 10 mL in 1 VIAL, PLASTIC (70069-506-01)

Ingredients (1)

cupric chloride (.4 mg/mL)

Linked Drug Pages (1)

Cupric Chloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "ea32e1b7-7c91-478e-9a8c-85f035431e19", "openfda": {"upc": ["0370069506011"], "unii": ["S2QG84156O"], "rxcui": ["204536"], "spl_set_id": ["361d30f2-3c97-4a6c-b252-7fa864d0a625"], "manufacturer_name": ["Somerset Therapeutics, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, PLASTIC in 1 CARTON (70069-506-25)  / 10 mL in 1 VIAL, PLASTIC (70069-506-01)", "package_ndc": "70069-506-25", "marketing_start_date": "20240514"}], "brand_name": "Cupric Chloride", "product_id": "70069-506_ea32e1b7-7c91-478e-9a8c-85f035431e19", "dosage_form": "INJECTION", "product_ndc": "70069-506", "generic_name": "Cupric Chloride", "labeler_name": "Somerset Therapeutics, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cupric Chloride", "active_ingredients": [{"name": "CUPRIC CHLORIDE", "strength": ".4 mg/mL"}], "application_number": "ANDA216113", "marketing_category": "ANDA", "marketing_start_date": "20240514", "listing_expiration_date": "20261231"}