Sodium Phosphate P 32

   
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Sodium Phosphate P 32


Drug - Sodium Phosphate P 32
The trade name of the product as shown on the labeling.

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

Active Ingredient(s) - Sodium Phosphate, P-32
Multiple ingredients are in alphabetical order.

Strength - 1.5mCi/VIAL
The potency of the active ingredient(s), Sodium Phosphate, P-32. May repeat for multiple part products.

Applicant - MALLINCKRODT
The firm name holding legal responsibility for Sodium Phosphate P 32. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 011777
The FDA assigned number to Sodium Phosphate P 32. Format is nnnnnn.

Product Number - 002
The FDA assigned number to identify Sodium Phosphate P 32. 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 Sodium Phosphate P 32 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 Sodium Phosphate P 32. 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 Sodium Phosphate P 32 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 Sodium Phosphate P 32.

Sodium Phosphate P 32