Milrinone Lactose In 5% Dextrose

   
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Milrinone Lactose In 5% Dextrose


Drug - Milrinone Lactose In 5% Dextrose
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) - Milrinone Lactate
Multiple ingredients are in alphabetical order.

Strength - EQ 20MG BASE/100ML
The potency of the active ingredient(s), Milrinone Lactate. May repeat for multiple part products.

Applicant - BAXTER HLTHCARE
The firm name holding legal responsibility for Milrinone Lactose In 5% Dextrose. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 076259
The FDA assigned number to Milrinone Lactose In 5% Dextrose. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Milrinone Lactose In 5% Dextrose. Each strength is a separate product. May repeat for multiple part products. Format is nnn.

Therapeutic Equivalence (TE) Code - AP
The TE Code indicates the therapeutic equivalence rating of generic to innovator Rx products.

Approval Date - Aug 8, 2002
The date Milrinone Lactose In 5% Dextrose 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 Milrinone Lactose In 5% Dextrose. 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 Milrinone Lactose In 5% Dextrose is in. Format is RX, OTC, DISCN.

Applicant Full Name - Baxter Healthcare Corp Anesthesia And Critical Care
The full name of the firm holding legal responsibility for the new application of Milrinone Lactose In 5% Dextrose.

Milrinone Lactose In 5% Dextrose