Drug - Aminophylline
The trade name of the product as shown on the labeling.

The product dosage form and route separated by a semi-colon.

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

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

The firm name holding legal responsibility for Aminophylline. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 088182
The FDA assigned number to Aminophylline. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Aminophylline. 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 - Mar 31, 1983
The date Aminophylline 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 Aminophylline. 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 Aminophylline is in. Format is RX, OTC, DISCN.

Applicant Full Name - Duramed Pharmaceuticals Inc Sub Barr Laboratories Inc
The full name of the firm holding legal responsibility for the new application of Aminophylline.