Children's Advil-flavored

   
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Children's Advil-flavored


Drug - Children's Advil-flavored
The trade name of the product as shown on the labeling.

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

Active Ingredient(s) - Ibuprofen
Multiple ingredients are in alphabetical order.

Strength - 100MG/5ML
The potency of the active ingredient(s), Ibuprofen. May repeat for multiple part products.

Applicant - WYETH CONS
The firm name holding legal responsibility for Children's Advil-flavored. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 020589
The FDA assigned number to Children's Advil-flavored. Format is nnnnnn.

Product Number - 002
The FDA assigned number to identify Children's Advil-flavored. 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 - Nov 7, 1997
The date Children's Advil-flavored 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 Children's Advil-flavored. The RLD identifies the product Abbreviated New Drug Applications (ANDA) use as a reference. Format is Yes or No.

Type - OTC
The group or category of approved drugs Children's Advil-flavored is in. Format is RX, OTC, DISCN.

Applicant Full Name - Wyeth Consumer Healthcare
The full name of the firm holding legal responsibility for the new application of Children's Advil-flavored.

Children's Advil-flavored