Propantheline Bromide

   
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Propantheline Bromide


Drug - Propantheline Bromide
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) - Propantheline Bromide
Multiple ingredients are in alphabetical order.

Strength - 15MG
The potency of the active ingredient(s), Propantheline Bromide. May repeat for multiple part products.

Applicant - HEATHER
The firm name holding legal responsibility for Propantheline Bromide. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 085780
The FDA assigned number to Propantheline Bromide. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Propantheline Bromide. 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 Propantheline Bromide 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 Propantheline Bromide. 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 Propantheline Bromide is in. Format is RX, OTC, DISCN.

Applicant Full Name - Heather Drug Co Inc
The full name of the firm holding legal responsibility for the new application of Propantheline Bromide.

Propantheline Bromide