Propoxyphene Napsylate And Acetaminophen

   
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Propoxyphene Napsylate And Acetaminophen


Drug - Propoxyphene Napsylate And Acetaminophen
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; Propoxyphene Napsylate
Multiple ingredients are in alphabetical order.

Strength - 500MG;100MG
The potency of the active ingredient(s), Acetaminophen; Propoxyphene Napsylate. May repeat for multiple part products.

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

New Drug Application (NDA) Number - 076750
The FDA assigned number to Propoxyphene Napsylate And Acetaminophen. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Propoxyphene Napsylate And Acetaminophen. 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 - Jun 28, 2004
The date Propoxyphene Napsylate And Acetaminophen 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 Propoxyphene Napsylate And Acetaminophen. 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 Propoxyphene Napsylate And Acetaminophen 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 Propoxyphene Napsylate And Acetaminophen.

Propoxyphene Napsylate And Acetaminophen