Tetrex

   
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Tetrex


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

Dosage - CAPSULE; ORAL
The product dosage form and route separated by a semi-colon.

Active Ingredient(s) - Tetracycline Phosphate Complex
Multiple ingredients are in alphabetical order.

Strength - EQ 500MG HCL
The potency of the active ingredient(s), Tetracycline Phosphate Complex. May repeat for multiple part products.

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

New Drug Application (NDA) Number - 061653
The FDA assigned number to Tetrex. Format is nnnnnn.

Product Number - 003
The FDA assigned number to identify Tetrex. 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 Tetrex 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 Tetrex. 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 Tetrex is in. Format is RX, OTC, DISCN.

Applicant Full Name - Bristol Laboratories Inc Div Bristol Myers Co
The full name of the firm holding legal responsibility for the new application of Tetrex.

Tetrex