Acetaminophen And Butalbital And Caffeine

   
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Acetaminophen And Butalbital And Caffeine


Drug - Acetaminophen And Butalbital And Caffeine
The trade name of the product as shown on the labeling.

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

Active Ingredient(s) - Acetaminophen; Butalbital; Caffeine
Multiple ingredients are in alphabetical order.

Strength - 325MG/15ML;50MG/15ML;40MG/15ML
The potency of the active ingredient(s), Acetaminophen; Butalbital; Caffeine. May repeat for multiple part products.

Applicant - MIKART
The firm name holding legal responsibility for Acetaminophen And Butalbital And Caffeine. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 040387
The FDA assigned number to Acetaminophen And Butalbital And Caffeine. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Acetaminophen And Butalbital And Caffeine. 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 31, 2003
The date Acetaminophen And Butalbital And Caffeine 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) - Yes
The pioneer or innovator of Acetaminophen And Butalbital And Caffeine. 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 Acetaminophen And Butalbital And Caffeine is in. Format is RX, OTC, DISCN.

Applicant Full Name - Mikart Inc
The full name of the firm holding legal responsibility for the new application of Acetaminophen And Butalbital And Caffeine.

Acetaminophen And Butalbital And Caffeine