Geocillin

   
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Geocillin


Drug - Geocillin
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) - Carbenicillin Indanyl Sodium
Multiple ingredients are in alphabetical order.

Strength - EQ 382MG BASE
The potency of the active ingredient(s), Carbenicillin Indanyl Sodium. May repeat for multiple part products.

Applicant - PFIZER
The firm name holding legal responsibility for Geocillin. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 050435
The FDA assigned number to Geocillin. Format is nnnnnn.

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

Applicant Full Name - Pfizer Laboratories Div Pfizer Inc
The full name of the firm holding legal responsibility for the new application of Geocillin.

Geocillin