Bethanechol Chloride

   
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Bethanechol Chloride


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

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

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

Strength - 25MG
The potency of the active ingredient(s), Bethanechol Chloride. May repeat for multiple part products.

Applicant - UPSHER SMITH
The firm name holding legal responsibility for Bethanechol Chloride. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 040635
The FDA assigned number to Bethanechol Chloride. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Bethanechol Chloride. 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 - Jun 1, 2005
The date Bethanechol Chloride 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 Bethanechol Chloride. 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 Bethanechol Chloride is in. Format is RX, OTC, DISCN.

Applicant Full Name - Upsher Smith Laboratories Inc
The full name of the firm holding legal responsibility for the new application of Bethanechol Chloride.

Bethanechol Chloride