Butalbital, Acetaminophen And Caffeine

   
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Butalbital, Acetaminophen And Caffeine


Drug - Butalbital, Acetaminophen And Caffeine
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; Butalbital; Caffeine
Multiple ingredients are in alphabetical order.

Strength - 500MG;50MG;40MG
The potency of the active ingredient(s), Acetaminophen; Butalbital; Caffeine. May repeat for multiple part products.

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

New Drug Application (NDA) Number - 040513
The FDA assigned number to Butalbital, Acetaminophen And Caffeine. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Butalbital, Acetaminophen And Caffeine. Each strength is a separate product. May repeat for multiple part products. Format is nnn.

Therapeutic Equivalence (TE) Code - AB
The TE Code indicates the therapeutic equivalence rating of generic to innovator Rx products.

Approval Date - Aug 25, 2003
The date Butalbital, Acetaminophen 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) - No
The pioneer or innovator of Butalbital, Acetaminophen 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 Butalbital, Acetaminophen And Caffeine is in. Format is RX, OTC, DISCN.

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

Butalbital, Acetaminophen And Caffeine