Sodium Chromate Cr 51

   
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Sodium Chromate Cr 51


Drug - Sodium Chromate Cr 51
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) - Sodium Chromate, Cr-51
Multiple ingredients are in alphabetical order.

Strength - 100uCi/ML
The potency of the active ingredient(s), Sodium Chromate, Cr-51. May repeat for multiple part products.

Applicant - MALLINCKRODT
The firm name holding legal responsibility for Sodium Chromate Cr 51. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 016708
The FDA assigned number to Sodium Chromate Cr 51. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Sodium Chromate Cr 51. 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 Chromate Cr 51 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 Chromate Cr 51. 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 Sodium Chromate Cr 51 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 Chromate Cr 51.

Sodium Chromate Cr 51