Humulin Br

   
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Humulin Br


Drug - Humulin Br
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 Recombinant Human
Multiple ingredients are in alphabetical order.

Strength - 100 UNITS/ML
The potency of the active ingredient(s), Insulin Recombinant Human. May repeat for multiple part products.

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

New Drug Application (NDA) Number - 019529
The FDA assigned number to Humulin Br. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Humulin Br. 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 - Apr 28, 1986
The date Humulin Br 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 Humulin Br. 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 Humulin Br 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 Humulin Br.

Humulin Br