Dicurin Procaine

   
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Dicurin Procaine


Drug - Dicurin Procaine
The trade name of the product as shown on the labeling.

Dosage - INJECTABLE; INJECTION
The product dosage form and route separated by a semi-colon.

Active Ingredient(s) - Procaine Merethoxylline; Theophylline
Multiple ingredients are in alphabetical order.

Strength - 100MG/ML;50MG/ML
The potency of the active ingredient(s), Procaine Merethoxylline; Theophylline. May repeat for multiple part products.

Applicant - LILLY
The firm name holding legal responsibility for Dicurin Procaine. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 008869
The FDA assigned number to Dicurin Procaine. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Dicurin Procaine. 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 Dicurin Procaine 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 Dicurin Procaine. 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 Dicurin Procaine is in. Format is RX, OTC, DISCN.

Applicant Full Name - Eli Lilly And Co
The full name of the firm holding legal responsibility for the new application of Dicurin Procaine.

Dicurin Procaine