Heparin Sodium 12,500 Units In Sodium Chloride 0.9%

   
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Heparin Sodium 12,500 Units In Sodium Chloride 0.9%


Drug - Heparin Sodium 12,500 Units In Sodium Chloride 0.9%
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) - Heparin Sodium
Multiple ingredients are in alphabetical order.

Strength - 5,000 UNITS/100ML
The potency of the active ingredient(s), Heparin Sodium. May repeat for multiple part products.

Applicant - HOSPIRA
The firm name holding legal responsibility for Heparin Sodium 12,500 Units In Sodium Chloride 0.9%. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 018911
The FDA assigned number to Heparin Sodium 12,500 Units In Sodium Chloride 0.9%. Format is nnnnnn.

Product Number - 005
The FDA assigned number to identify Heparin Sodium 12,500 Units In Sodium Chloride 0.9%. 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 - Jan 30, 1985
The date Heparin Sodium 12,500 Units In Sodium Chloride 0.9% 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) - No
The pioneer or innovator of Heparin Sodium 12,500 Units In Sodium Chloride 0.9%. The RLD identifies the product Abbreviated New Drug Applications (ANDA) use as a reference. Format is Yes or No.

Type - DISCN
The group or category of approved drugs Heparin Sodium 12,500 Units In Sodium Chloride 0.9% 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 Heparin Sodium 12,500 Units In Sodium Chloride 0.9%.

Heparin Sodium 12,500 Units In Sodium Chloride 0.9%


Heparin Sodium 10,000 Units In Sodium Chloride 0.45% 10,000 Units/100ml Injectable; Injection
Heparin Sodium 10,000 Units In Sodium Chloride 0.9% 10,000 Units/100ml Injectable; Injection
Heparin Sodium 10,000 Units In Sodium Chloride 0.9% 10,000 Units/100ml Injectable; Injection
Heparin Sodium 12,500 Units In Dextrose 5% 5,000 Units/100ml Injectable; Injection
Heparin Sodium 12,500 Units In Dextrose 5% In Plastic Container 5,000 Units/100ml Injectable; Injection
Heparin Sodium 12,500 Units In Sodium Chloride 0.45% In Plastic Container 5,000 Units/100ml Injectable; Injection
Heparin Sodium 12,500 Units In Sodium Chloride 0.45% In Plastic Container 5,000 Units/100ml Injectable; Injection
Heparin Sodium 12,500 Units In Sodium Chloride 0.9% 5,000 Units/100ml Injectable; Injection
Heparin Sodium 10,000 Units In Dextrose 5% In Plastic Container 10,000 Units/100ml Injectable; Injection
Heparin Sodium 10,000 Units In Sodium Chloride 0.45% 10,000 Units/100ml Injectable; Injection

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