Codoxy

   
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Codoxy


Drug - Codoxy
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) - Aspirin; Oxycodone Hydrochloride; Oxycodone Terephthalate
Multiple ingredients are in alphabetical order.

Strength - 325MG;4.5MG;0.38MG
The potency of the active ingredient(s), Aspirin; Oxycodone Hydrochloride; Oxycodone Terephthalate. May repeat for multiple part products.

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

New Drug Application (NDA) Number - 087464
The FDA assigned number to Codoxy. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Codoxy. 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 - Jul 1, 1982
The date Codoxy 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 Codoxy. 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 Codoxy is in. Format is RX, OTC, DISCN.

Applicant Full Name - Halsey Drug Co Inc
The full name of the firm holding legal responsibility for the new application of Codoxy.

Codoxy