E-z Prep 220
Drug - E-z Prep 220
The trade name of the product as shown on the labeling.
Dosage -
SPONGE; TOPICAL
The product dosage form and route separated by a semi-colon.
Active Ingredient(s) -
Povidone-iodine
Multiple ingredients are in alphabetical order.
Strength -
5%
The potency of the active ingredient(s), Povidone-iodine. May repeat for multiple part products.
Applicant -
BECTON DICKINSON
The firm name holding legal responsibility for E-z Prep 220. The firm name is condensed to a maximum twenty character unique string.
New Drug Application (NDA) Number -
019382
The FDA assigned number to E-z Prep 220. Format is nnnnnn.
Product Number -
003
The FDA assigned number to identify E-z Prep 220. 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 -
Jul 25, 1989
The date E-z Prep 220 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 E-z Prep 220. The RLD identifies the product Abbreviated New Drug Applications (ANDA) use as a reference. Format is Yes or No.
Type -
OTC
The group or category of approved drugs E-z Prep 220 is in. Format is RX, OTC, DISCN.
Applicant Full Name -
Becton Dickinson And Co
The full name of the firm holding legal responsibility for the new application of E-z Prep 220.
E-z Prep 220
|
