Mannitol 10% In Plastic Container

   
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Mannitol 10% In Plastic Container


Drug - Mannitol 10% In Plastic Container
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) - Mannitol
Multiple ingredients are in alphabetical order.

Strength - 10GM/100ML
The potency of the active ingredient(s), Mannitol. May repeat for multiple part products.

Applicant - HOSPIRA
The firm name holding legal responsibility for Mannitol 10% In Plastic Container. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 019603
The FDA assigned number to Mannitol 10% In Plastic Container. Format is nnnnnn.

Product Number - 002
The FDA assigned number to identify Mannitol 10% In Plastic Container. 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 - Jan 8, 1987
The date Mannitol 10% In Plastic Container 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 Mannitol 10% In Plastic Container. 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 Mannitol 10% In Plastic Container is in. Format is RX, OTC, DISCN.

Applicant Full Name - Hospira Inc
The full name of the firm holding legal responsibility for the new application of Mannitol 10% In Plastic Container.

Mannitol 10% In Plastic Container