Pbz-sr

   
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Pbz-sr


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

Dosage - TABLET, EXTENDED RELEASE; ORAL
The product dosage form and route separated by a semi-colon.

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

Strength - 100MG
The potency of the active ingredient(s), Tripelennamine Hydrochloride. May repeat for multiple part products.

Applicant - NOVARTIS
The firm name holding legal responsibility for Pbz-sr. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 010533
The FDA assigned number to Pbz-sr. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Pbz-sr. 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 - Approved Prior to Jan 1, 1982
The date Pbz-sr 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 Pbz-sr. 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 Pbz-sr is in. Format is RX, OTC, DISCN.

Applicant Full Name - Novartis Pharmaceuticals Corp
The full name of the firm holding legal responsibility for the new application of Pbz-sr.

Pbz-sr