Acetaminophen And Codeine Phosphate

   
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Acetaminophen And Codeine Phosphate


Drug - Acetaminophen And Codeine Phosphate
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) - Acetaminophen; Codeine Phosphate
Multiple ingredients are in alphabetical order.

Strength - 300MG;15MG
The potency of the active ingredient(s), Acetaminophen; Codeine Phosphate. May repeat for multiple part products.

Applicant - MUTUAL PHARM
The firm name holding legal responsibility for Acetaminophen And Codeine Phosphate. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 085795
The FDA assigned number to Acetaminophen And Codeine Phosphate. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Acetaminophen And Codeine Phosphate. 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 - Approved Prior to Jan 1, 1982
The date Acetaminophen And Codeine Phosphate 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 Acetaminophen And Codeine Phosphate. 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 Acetaminophen And Codeine Phosphate 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 Acetaminophen And Codeine Phosphate.

Acetaminophen And Codeine Phosphate