FDA Product

CUPRIC CHLORIDE

Product approved by U.S. Food and Drug Administration (US)

Basic Information

Product Name

CUPRIC CHLORIDE

FDA Product Code

51754-0103

Regulatory Information

NDC Product Code

51754-0103

Application Number

ANDA212071

Marketing Category

C73584

Effective Date

May 16, 2019

Territorial Authority

USA

FDA Title

CUPRIC CHLORIDE INJECTION, USP – solution

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Version Number

1

Company Information

ManufacturerExela Pharma Sciences, LLC

DUNS Number

831274399

Active Ingredients

CUPRIC CHLORIDE

Quantity: 0.4 mg in 1 mL

Code: S2QG84156O

Class Code: ACTIM

SODIUM CHLORIDE

Code: 451W47IQ8X

Class Code: IACT

SODIUM HYDROXIDE

Code: 55X04QC32I

Class Code: IACT

HYDROCHLORIC ACID

Code: QTT17582CB

Class Code: IACT

Active Moieties

CUPRIC CATION

Code: 8CBV67279L

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