Minoxidil (for Men)

   
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Minoxidil (for Men)


Drug - Minoxidil (for Men)
The trade name of the product as shown on the labeling.

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

Active Ingredient(s) - Minoxidil
Multiple ingredients are in alphabetical order.

Strength - 2%
The potency of the active ingredient(s), Minoxidil. May repeat for multiple part products.

Applicant - COPLEY PHARM
The firm name holding legal responsibility for Minoxidil (for Men). The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 074500
The FDA assigned number to Minoxidil (for Men). Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Minoxidil (for Men). 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 - May 23, 1996
The date Minoxidil (for Men) 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 Minoxidil (for Men). 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 Minoxidil (for Men) is in. Format is RX, OTC, DISCN.

Applicant Full Name - Copley Pharmaceutical Inc
The full name of the firm holding legal responsibility for the new application of Minoxidil (for Men).

Minoxidil (for Men)