Oxycodone And Aspirin

   
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Oxycodone And Aspirin


Drug - Oxycodone And Aspirin
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 - MUTUAL PHARM
The firm name holding legal responsibility for Oxycodone And Aspirin. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 040260
The FDA assigned number to Oxycodone And Aspirin. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Oxycodone And Aspirin. 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 - Jul 17, 1998
The date Oxycodone And Aspirin 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 Oxycodone And Aspirin. 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 Oxycodone And Aspirin is in. Format is RX, OTC, DISCN.

Applicant Full Name - Mutual Pharmaceutical Co Inc
The full name of the firm holding legal responsibility for the new application of Oxycodone And Aspirin.

Oxycodone And Aspirin