Protamine Zinc And Iletin Ii

   
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Protamine Zinc And Iletin Ii


Drug - Protamine Zinc And 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 Susp Protamine Zinc Purified Beef
Multiple ingredients are in alphabetical order.

Strength - 100 UNITS/ML
The potency of the active ingredient(s), Insulin Susp Protamine Zinc Purified Beef. May repeat for multiple part products.

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

New Drug Application (NDA) Number - 018476
The FDA assigned number to Protamine Zinc And Iletin Ii. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Protamine Zinc And 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 Protamine Zinc And 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) - No
The pioneer or innovator of Protamine Zinc And Iletin Ii. 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 Protamine Zinc And 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 Protamine Zinc And Iletin Ii.

Protamine Zinc And Iletin Ii