Prevacid

   
Google
 
Web NewDrugInformation.com

Prevacid


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

Dosage - FOR SUSPENSION, DELAYED RELEASE; ORAL
The product dosage form and route separated by a semi-colon.

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

Strength - 30MG/PACKET
The potency of the active ingredient(s), Lansoprazole. May repeat for multiple part products.

Applicant - TAP PHARM
The firm name holding legal responsibility for Prevacid. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 021281
The FDA assigned number to Prevacid. Format is nnnnnn.

Product Number - 002
The FDA assigned number to identify Prevacid. 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, 2001
The date Prevacid 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 Prevacid. 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 Prevacid is in. Format is RX, OTC, DISCN.

Applicant Full Name - Tap Pharmaceutical Products Inc
The full name of the firm holding legal responsibility for the new application of Prevacid.

Prevacid