Heparin Lock Flush

   
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Heparin Lock Flush


Drug - Heparin Lock Flush
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) - Heparin Sodium
Multiple ingredients are in alphabetical order.

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

Applicant - SMITH AND NEPHEW
The firm name holding legal responsibility for Heparin Lock Flush. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 088581
The FDA assigned number to Heparin Lock Flush. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Heparin Lock Flush. 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 - Oct 25, 1984
The date Heparin Lock Flush 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 Heparin Lock Flush. 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 Heparin Lock Flush is in. Format is RX, OTC, DISCN.

Applicant Full Name - Smith And Nephew Solopak Div Smith And Nephew
The full name of the firm holding legal responsibility for the new application of Heparin Lock Flush.

Heparin Lock Flush