Myidyl

   
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Myidyl


Drug - Myidyl
The trade name of the product as shown on the labeling.

Dosage - SYRUP; ORAL
The product dosage form and route separated by a semi-colon.

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

Strength - 1.25MG/5ML
The potency of the active ingredient(s), Triprolidine Hydrochloride. May repeat for multiple part products.

Applicant - USL PHARMA
The firm name holding legal responsibility for Myidyl. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 087963
The FDA assigned number to Myidyl. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Myidyl. 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 - Jan 18, 1983
The date Myidyl 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 Myidyl. 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 Myidyl is in. Format is RX, OTC, DISCN.

Applicant Full Name - Usl Pharma Inc
The full name of the firm holding legal responsibility for the new application of Myidyl.

Myidyl