Iletin Ii

   
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Iletin Ii


Drug - Iletin Ii
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) - Insulin Purified Pork
Multiple ingredients are in alphabetical order.

Strength - 500 UNITS/ML
The potency of the active ingredient(s), Insulin Purified Pork. May repeat for multiple part products.

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

New Drug Application (NDA) Number - 018344
The FDA assigned number to Iletin Ii. Format is nnnnnn.

Product Number - 002
The FDA assigned number to identify Iletin Ii. 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 Iletin Ii 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 Iletin Ii. 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 Iletin Ii 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 Iletin Ii.

Iletin Ii