Albuterol Sulfate

   
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Albuterol Sulfate


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

Dosage - TABLET; ORAL
The product dosage form and route separated by a semi-colon.

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

Strength - EQ 4MG BASE
The potency of the active ingredient(s), Albuterol Sulfate. May repeat for multiple part products.

Applicant - WARNER CHILCOTT
The firm name holding legal responsibility for Albuterol Sulfate. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 072818
The FDA assigned number to Albuterol Sulfate. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Albuterol Sulfate. 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 9, 1990
The date Albuterol Sulfate 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 Albuterol Sulfate. 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 Albuterol Sulfate is in. Format is RX, OTC, DISCN.

Applicant Full Name - Warner Chilcott Div Warner Lambert Co
The full name of the firm holding legal responsibility for the new application of Albuterol Sulfate.

Albuterol Sulfate