cupric chloride

Generic: cupric chloride

Labeler: exela pharma sciences, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cupric chloride
Generic Name cupric chloride
Labeler exela pharma sciences, llc
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

cupric chloride .4 mg/mL

Manufacturer
Exela Pharma Sciences, LLC

Identifiers & Regulatory

Product NDC 51754-0103
Product ID 51754-0103_18dc9e1c-b9db-4160-96f7-8c4391bcf8c9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212071
Listing Expiration 2026-12-31
Marketing Start 2023-02-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 517540103
Hyphenated Format 51754-0103

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 ANDA212071 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • .4 mg/mL
source: ndc
Packaging
  • 10 VIAL, SINGLE-DOSE in 1 CARTON (51754-0103-3) / 10 mL in 1 VIAL, SINGLE-DOSE
  • 25 VIAL, SINGLE-DOSE in 1 CARTON (51754-0103-4) / 10 mL in 1 VIAL, SINGLE-DOSE
source: ndc

Packages (2)

51754-0103-3 10 VIAL, SINGLE-DOSE in 1 CARTON (51754-0103-3) / 10 mL in 1 VIAL, SINGLE-DOSE 51754-0103-4 25 VIAL, SINGLE-DOSE in 1 CARTON (51754-0103-4) / 10 mL in 1 VIAL, SINGLE-DOSE

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": "18dc9e1c-b9db-4160-96f7-8c4391bcf8c9", "openfda": {"unii": ["S2QG84156O"], "rxcui": ["204536"], "spl_set_id": ["daaa6f3a-148e-4f1c-bd44-bb2242145b88"], "manufacturer_name": ["Exela Pharma Sciences, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (51754-0103-3)  / 10 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "51754-0103-3", "marketing_start_date": "20230201"}, {"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (51754-0103-4)  / 10 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "51754-0103-4", "marketing_start_date": "20230201"}], "brand_name": "CUPRIC CHLORIDE", "product_id": "51754-0103_18dc9e1c-b9db-4160-96f7-8c4391bcf8c9", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "51754-0103", "generic_name": "cupric chloride", "labeler_name": "Exela Pharma Sciences, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CUPRIC CHLORIDE", "active_ingredients": [{"name": "CUPRIC CHLORIDE", "strength": ".4 mg/mL"}], "application_number": "ANDA212071", "marketing_category": "ANDA", "marketing_start_date": "20230201", "listing_expiration_date": "20261231"}