Ceclor Cd

   
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Ceclor Cd


Drug - Ceclor Cd
The trade name of the product as shown on the labeling.

Dosage - TABLET, EXTENDED RELEASE; ORAL
The product dosage form and route separated by a semi-colon.

Active Ingredient(s) - Cefaclor
Multiple ingredients are in alphabetical order.

Strength - EQ 375MG BASE
The potency of the active ingredient(s), Cefaclor. May repeat for multiple part products.

Applicant - LILLY
The firm name holding legal responsibility for Ceclor Cd. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 050673
The FDA assigned number to Ceclor Cd. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Ceclor Cd. 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 - Jun 28, 1996
The date Ceclor Cd 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 Ceclor Cd. 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 Ceclor Cd is in. Format is RX, OTC, DISCN.

Applicant Full Name - Eli Lilly And Co
The full name of the firm holding legal responsibility for the new application of Ceclor Cd.

Ceclor Cd