Corphed

   
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Corphed


Drug - Corphed
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) - Pseudoephedrine Hydrochloride; Triprolidine Hydrochloride
Multiple ingredients are in alphabetical order.

Strength - 60MG;2.5MG
The potency of the active ingredient(s), Pseudoephedrine Hydrochloride; Triprolidine Hydrochloride. May repeat for multiple part products.

Applicant - SANDOZ
The firm name holding legal responsibility for Corphed. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 088602
The FDA assigned number to Corphed. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Corphed. 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 - Apr 11, 1985
The date Corphed 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 Corphed. 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 Corphed is in. Format is RX, OTC, DISCN.

Applicant Full Name - Sandoz Inc
The full name of the firm holding legal responsibility for the new application of Corphed.

Corphed