Ona Mast
Drug - Ona Mast
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) -
Phentermine Hydrochloride
Multiple ingredients are in alphabetical order.
Strength -
8MG
The potency of the active ingredient(s), Phentermine Hydrochloride. May repeat for multiple part products.
Applicant -
MAST MM
The firm name holding legal responsibility for Ona Mast. The firm name is condensed to a maximum twenty character unique string.
New Drug Application (NDA) Number -
086260
The FDA assigned number to Ona Mast. Format is nnnnnn.
Product Number -
001
The FDA assigned number to identify Ona Mast. 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 -
Approved Prior to Jan 1, 1982
The date Ona Mast 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 Ona Mast. 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 Ona Mast is in. Format is RX, OTC, DISCN.
Applicant Full Name -
Mm Mast And Co
The full name of the firm holding legal responsibility for the new application of Ona Mast.
Ona Mast
|
