Md-gastroview

   
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Md-gastroview


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

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

Active Ingredient(s) - Diatrizoate Meglumine; Diatrizoate Sodium
Multiple ingredients are in alphabetical order.

Strength - 66%;10%
The potency of the active ingredient(s), Diatrizoate Meglumine; Diatrizoate Sodium. May repeat for multiple part products.

Applicant - MALLINCKRODT
The firm name holding legal responsibility for Md-gastroview. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 087388
The FDA assigned number to Md-gastroview. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Md-gastroview. Each strength is a separate product. May repeat for multiple part products. Format is nnn.

Therapeutic Equivalence (TE) Code - AA
The TE Code indicates the therapeutic equivalence rating of generic to innovator Rx products.

Approval Date - Approved Prior to Jan 1, 1982
The date Md-gastroview 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 Md-gastroview. 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 Md-gastroview is in. Format is RX, OTC, DISCN.

Applicant Full Name - Mallinckrodt Medical Inc
The full name of the firm holding legal responsibility for the new application of Md-gastroview.

Md-gastroview