Ibuprohm Cold And Sinus

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Ibuprohm Cold And Sinus

Drug - Ibuprohm Cold And Sinus
The trade name of the product as shown on the labeling.

The product dosage form and route separated by a semi-colon.

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

Strength - 200MG;30MG
The potency of the active ingredient(s), Ibuprofen; Pseudoephedrine Hydrochloride. May repeat for multiple part products.

Applicant - OHM LABS
The firm name holding legal responsibility for Ibuprohm Cold And Sinus. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 074567
The FDA assigned number to Ibuprohm Cold And Sinus. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Ibuprohm Cold And Sinus. 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 - Apr 17, 2001
The date Ibuprohm Cold And Sinus 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 Ibuprohm Cold And Sinus. 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 Ibuprohm Cold And Sinus is in. Format is RX, OTC, DISCN.

Applicant Full Name - Ohm Laboratories Inc
The full name of the firm holding legal responsibility for the new application of Ibuprohm Cold And Sinus.

Ibuprohm Cold And Sinus