Qvar 40
Drug - Qvar 40
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) -
Beclomethasone Dipropionate
Multiple ingredients are in alphabetical order.
Strength -
0.04MG/INH
The potency of the active ingredient(s), Beclomethasone Dipropionate. May repeat for multiple part products.
Applicant -
3M
The firm name holding legal responsibility for Qvar 40. The firm name is condensed to a maximum twenty character unique string.
New Drug Application (NDA) Number -
020911
The FDA assigned number to Qvar 40. Format is nnnnnn.
Product Number -
002
The FDA assigned number to identify Qvar 40. 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 -
Sep 15, 2000
The date Qvar 40 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 Qvar 40. 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 Qvar 40 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 Qvar 40.
Qvar 40
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