Nulytely

   
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Nulytely


Drug - Nulytely
The trade name of the product as shown on the labeling.

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

Active Ingredient(s) - Polyethylene Glycol 3350; Potassium Chloride; Sodium Bicarbonate; Sodium Chloride
Multiple ingredients are in alphabetical order.

Strength - 420GM/BOT;1.48GM/BOT;5.72GM/BOT;11.2GM/BOT
The potency of the active ingredient(s), Polyethylene Glycol 3350; Potassium Chloride; Sodium Bicarbonate; Sodium Chloride. May repeat for multiple part products.

Applicant - BRAINTREE
The firm name holding legal responsibility for Nulytely. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 019797
The FDA assigned number to Nulytely. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Nulytely. Each strength is a separate product. May repeat for multiple part products. Format is nnn.

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

Approval Date - Apr 22, 1991
The date Nulytely 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 Nulytely. 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 Nulytely is in. Format is RX, OTC, DISCN.

Applicant Full Name - Braintree Laboratories Inc
The full name of the firm holding legal responsibility for the new application of Nulytely.

Nulytely