Prosol 20% Sulfite Free In Plastic Container

   
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Prosol 20% Sulfite Free In Plastic Container


Drug - Prosol 20% Sulfite Free 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) - Amino Acids
Multiple ingredients are in alphabetical order.

Strength - 20% (20GM/100ML)
The potency of the active ingredient(s), Amino Acids. May repeat for multiple part products.

Applicant - BAXTER HLTHCARE
The firm name holding legal responsibility for Prosol 20% Sulfite Free In Plastic Container. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 020849
The FDA assigned number to Prosol 20% Sulfite Free In Plastic Container. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Prosol 20% Sulfite Free In Plastic Container. 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 - Aug 26, 1998
The date Prosol 20% Sulfite Free 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) - Yes
The pioneer or innovator of Prosol 20% Sulfite Free 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 Prosol 20% Sulfite Free In Plastic Container is in. Format is RX, OTC, DISCN.

Applicant Full Name - Baxter Healthcare Internati0nal Specialty Therapies Div
The full name of the firm holding legal responsibility for the new application of Prosol 20% Sulfite Free In Plastic Container.

Prosol 20% Sulfite Free In Plastic Container