Orphenadrine Citrate, Aspirin, And Caffeine

   
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Orphenadrine Citrate, Aspirin, And Caffeine


Drug - Orphenadrine Citrate, Aspirin, 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) - Aspirin; Caffeine; Orphenadrine Citrate
Multiple ingredients are in alphabetical order.

Strength - 770MG;60MG;50MG
The potency of the active ingredient(s), Aspirin; Caffeine; Orphenadrine Citrate. May repeat for multiple part products.

Applicant - SANDOZ
The firm name holding legal responsibility for Orphenadrine Citrate, Aspirin, And Caffeine. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 074654
The FDA assigned number to Orphenadrine Citrate, Aspirin, And Caffeine. Format is nnnnnn.

Product Number - 002
The FDA assigned number to identify Orphenadrine Citrate, Aspirin, 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 - Dec 31, 1996
The date Orphenadrine Citrate, Aspirin, 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 Orphenadrine Citrate, Aspirin, 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 Orphenadrine Citrate, Aspirin, And Caffeine is in. Format is RX, OTC, DISCN.

Applicant Full Name - Sandoz Inc
The full name of the firm holding legal responsibility for the new application of Orphenadrine Citrate, Aspirin, And Caffeine.

Orphenadrine Citrate, Aspirin, And Caffeine