Provocholine

   
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Provocholine


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

Dosage - FOR SOLUTION; INHALATION
The product dosage form and route separated by a semi-colon.

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

Strength - 100MG/VIAL
The potency of the active ingredient(s), Methacholine Chloride. May repeat for multiple part products.

Applicant - METHAPHARM
The firm name holding legal responsibility for Provocholine. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 019193
The FDA assigned number to Provocholine. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Provocholine. 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 - Oct 31, 1986
The date Provocholine 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) - Yes
The pioneer or innovator of Provocholine. 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 Provocholine is in. Format is RX, OTC, DISCN.

Applicant Full Name - Methapharm Inc
The full name of the firm holding legal responsibility for the new application of Provocholine.

Provocholine