Duo-medihaler

   
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Duo-medihaler


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

Dosage - AEROSOL, METERED; INHALATION
The product dosage form and route separated by a semi-colon.

Active Ingredient(s) - Isoproterenol Hydrochloride; Phenylephrine Bitartrate
Multiple ingredients are in alphabetical order.

Strength - 0.16MG/INH;0.24MG/INH
The potency of the active ingredient(s), Isoproterenol Hydrochloride; Phenylephrine Bitartrate. May repeat for multiple part products.

Applicant - 3M
The firm name holding legal responsibility for Duo-medihaler. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 013296
The FDA assigned number to Duo-medihaler. Format is nnnnnn.

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

Applicant Full Name - 3m Pharmaceuticals Inc
The full name of the firm holding legal responsibility for the new application of Duo-medihaler.

Duo-medihaler