Drug - Ibuprohm
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) -
Multiple ingredients are in alphabetical order.
The potency of the active ingredient(s), Ibuprofen. May repeat for multiple part products.
The firm name holding legal responsibility for Ibuprohm. The firm name is condensed to a maximum twenty character unique string.
New Drug Application (NDA) Number -
The FDA assigned number to Ibuprohm. Format is nnnnnn.
Product Number -
The FDA assigned number to identify Ibuprohm. 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 -
Dec 1, 1986
The date Ibuprohm 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) -
The pioneer or innovator of Ibuprohm. The RLD identifies the product Abbreviated New Drug Applications (ANDA) use as a reference. Format is Yes or No.
The group or category of approved drugs Ibuprohm is in. Format is RX, OTC, DISCN.
Applicant Full Name -
Ohm Laboratories Inc
The full name of the firm holding legal responsibility for the new application of Ibuprohm.