Product Information on Physiosol In Plastic Container 30MG/100ML;37MG/100ML;222MG/100ML;526MG/100ML;502MG/100ML

Dosage - SOLUTION; IRRIGATION
The product dosage form and route separated by a semi-colon.

Active Ingredient(s) - Magnesium Chloride; Potassium Chloride; Sodium Acetate; Sodium Chloride; Sodium Gluconate
Multiple ingredients are in alphabetical order.

Strength - 30MG/100ML;37MG/100ML;222MG/100ML;526MG/100ML;502MG/100ML
The potency of the active ingredient(s), Magnesium Chloride; Potassium Chloride; Sodium Acetate; Sodium Chloride; Sodium Gluconate. May repeat for multiple part products.

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

New Drug Application (NDA) Number - 017637
The FDA assigned number to Physiosol In Plastic Container. Format is nnnnnn.

Product Number - 002
The FDA assigned number to identify Physiosol 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 - Jul 8, 1982
The date Physiosol 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 Physiosol 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 Physiosol 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 Physiosol In Plastic Container.

Physiosol In Plastic Container

NewDrugInformation