Ferrous Citrate Fe 59

   
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Ferrous Citrate Fe 59


Drug - Ferrous Citrate Fe 59
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) - Ferrous Citrate, Fe-59
Multiple ingredients are in alphabetical order.

Strength - 25uCi/ML
The potency of the active ingredient(s), Ferrous Citrate, Fe-59. May repeat for multiple part products.

Applicant - MALLINCKRODT
The firm name holding legal responsibility for Ferrous Citrate Fe 59. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 016729
The FDA assigned number to Ferrous Citrate Fe 59. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Ferrous Citrate Fe 59. 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 Ferrous Citrate Fe 59 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 Ferrous Citrate Fe 59. 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 Ferrous Citrate Fe 59 is in. Format is RX, OTC, DISCN.

Applicant Full Name - Mallinckrodt Inc
The full name of the firm holding legal responsibility for the new application of Ferrous Citrate Fe 59.

Ferrous Citrate Fe 59