Lidocaine And Prilocaine

   
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Lidocaine And Prilocaine


Drug - Lidocaine And Prilocaine
The trade name of the product as shown on the labeling.

Dosage - CREAM; TOPICAL
The product dosage form and route separated by a semi-colon.

Active Ingredient(s) - Lidocaine; Prilocaine
Multiple ingredients are in alphabetical order.

Strength - 2.5%;2.5%
The potency of the active ingredient(s), Lidocaine; Prilocaine. May repeat for multiple part products.

Applicant - HI TECH PHARMA
The firm name holding legal responsibility for Lidocaine And Prilocaine. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 076290
The FDA assigned number to Lidocaine And Prilocaine. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Lidocaine And Prilocaine. Each strength is a separate product. May repeat for multiple part products. Format is nnn.

Therapeutic Equivalence (TE) Code - AB
The TE Code indicates the therapeutic equivalence rating of generic to innovator Rx products.

Approval Date - Sep 25, 2003
The date Lidocaine And Prilocaine 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 Lidocaine And Prilocaine. 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 Lidocaine And Prilocaine is in. Format is RX, OTC, DISCN.

Applicant Full Name - Hi Tech Pharmacal Co Inc
The full name of the firm holding legal responsibility for the new application of Lidocaine And Prilocaine.

Lidocaine And Prilocaine