Midodrine Hcl

   
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Midodrine Hcl


Drug - Midodrine Hcl
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) - Midodrine Hydrochloride
Multiple ingredients are in alphabetical order.

Strength - 10MG
The potency of the active ingredient(s), Midodrine Hydrochloride. May repeat for multiple part products.

Applicant - MYLAN
The firm name holding legal responsibility for Midodrine Hcl. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 076577
The FDA assigned number to Midodrine Hcl. Format is nnnnnn.

Product Number - 003
The FDA assigned number to identify Midodrine Hcl. Each strength is a separate product. May repeat for multiple part products. Format is nnn.

Therapeutic Equivalence (TE) Code - AB
The TE Code indicates the therapeutic equivalence rating of generic to innovator Rx products.

Approval Date - Sep 10, 2003
The date Midodrine Hcl 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 Midodrine Hcl. 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 Midodrine Hcl is in. Format is RX, OTC, DISCN.

Applicant Full Name - Mylan Pharmaceuticals Inc
The full name of the firm holding legal responsibility for the new application of Midodrine Hcl.

Midodrine Hcl