Parafon Forte Dsc
Drug - Parafon Forte Dsc
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) -
Chlorzoxazone
Multiple ingredients are in alphabetical order.
Strength -
500MG
The potency of the active ingredient(s), Chlorzoxazone. May repeat for multiple part products.
Applicant -
ORTHO MCNEIL PHARM
The firm name holding legal responsibility for Parafon Forte Dsc. The firm name is condensed to a maximum twenty character unique string.
New Drug Application (NDA) Number -
011529
The FDA assigned number to Parafon Forte Dsc. Format is nnnnnn.
Product Number -
002
The FDA assigned number to identify Parafon Forte Dsc. Each strength is a separate product. May repeat for multiple part products. Format is nnn.
Therapeutic Equivalence (TE) Code -
AA
The TE Code indicates the therapeutic equivalence rating of generic to innovator Rx products.
Approval Date -
Jun 15, 1987
The date Parafon Forte Dsc 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 Parafon Forte Dsc. 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 Parafon Forte Dsc is in. Format is RX, OTC, DISCN.
Applicant Full Name -
Ortho Mcneil Pharmaceutical Inc
The full name of the firm holding legal responsibility for the new application of Parafon Forte Dsc.
Parafon Forte Dsc
|
