Cupric Chloride In Plastic Container

   
Google
 
Web NewDrugInformation.com

Cupric Chloride In Plastic Container


Drug - Cupric Chloride In Plastic Container
The trade name of the product as shown on the labeling.

Dosage - INJECTABLE; INJECTION
The product dosage form and route separated by a semi-colon.

Active Ingredient(s) - Cupric Chloride
Multiple ingredients are in alphabetical order.

Strength - EQ 0.4MG COPPER/ML
The potency of the active ingredient(s), Cupric Chloride. May repeat for multiple part products.

Applicant - HOSPIRA
The firm name holding legal responsibility for Cupric Chloride In Plastic Container. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 018960
The FDA assigned number to Cupric Chloride In Plastic Container. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Cupric Chloride In Plastic Container. Each strength is a separate product. May repeat for multiple part products. Format is nnn.

Therapeutic Equivalence (TE) Code -
The TE Code indicates the therapeutic equivalence rating of generic to innovator Rx products.

Approval Date - Jun 26, 1986
The date Cupric Chloride In Plastic Container was approved as stated in the FDA approval letter to the applicant. The format is Mmm dd, yyyy. Products approved prior to the January 1, 1982 contain the phrase: "Approved prior to Jan 1, 1982".

Reference Listed Drug (RLD) - Yes
The pioneer or innovator of Cupric Chloride In Plastic Container. The RLD identifies the product Abbreviated New Drug Applications (ANDA) use as a reference. Format is Yes or No.

Type - RX
The group or category of approved drugs Cupric Chloride In Plastic Container is in. Format is RX, OTC, DISCN.

Applicant Full Name - Hospira Inc
The full name of the firm holding legal responsibility for the new application of Cupric Chloride In Plastic Container.

Cupric Chloride In Plastic Container