Ferrlecit

   
Google
 
Web NewDrugInformation.com

Ferrlecit


Drug - Ferrlecit
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 Ferric Gluconate Complex
Multiple ingredients are in alphabetical order.

Strength - 62.5MG/5ML
The potency of the active ingredient(s), Sodium Ferric Gluconate Complex. May repeat for multiple part products.

Applicant - WATSON PHARMS
The firm name holding legal responsibility for Ferrlecit. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 020955
The FDA assigned number to Ferrlecit. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Ferrlecit. 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 - Feb 18, 1999
The date Ferrlecit 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 Ferrlecit. 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 Ferrlecit is in. Format is RX, OTC, DISCN.

Applicant Full Name - Watson Pharmaceuticals Inc
The full name of the firm holding legal responsibility for the new application of Ferrlecit.

Ferrlecit