Aminophylline In Sodium Chloride 0.45%

   
Google
 
Web NewDrugInformation.com

Aminophylline In Sodium Chloride 0.45%


Drug - Aminophylline In Sodium Chloride 0.45%
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) - Aminophylline
Multiple ingredients are in alphabetical order.

Strength - 200MG/100ML
The potency of the active ingredient(s), Aminophylline. May repeat for multiple part products.

Applicant - HOSPIRA
The firm name holding legal responsibility for Aminophylline In Sodium Chloride 0.45%. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 088147
The FDA assigned number to Aminophylline In Sodium Chloride 0.45%. Format is nnnnnn.

Product Number - 003
The FDA assigned number to identify Aminophylline In Sodium Chloride 0.45%. 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 - May 3, 1983
The date Aminophylline In Sodium Chloride 0.45% 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 Aminophylline In Sodium Chloride 0.45%. 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 Aminophylline In Sodium Chloride 0.45% 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 Aminophylline In Sodium Chloride 0.45%.

Aminophylline In Sodium Chloride 0.45%