Beta-val

   
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Beta-val


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

Dosage - OINTMENT; TOPICAL
The product dosage form and route separated by a semi-colon.

Active Ingredient(s) - Betamethasone Valerate
Multiple ingredients are in alphabetical order.

Strength - EQ 0.1% BASE
The potency of the active ingredient(s), Betamethasone Valerate. May repeat for multiple part products.

Applicant - TEVA
The firm name holding legal responsibility for Beta-val. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 070069
The FDA assigned number to Beta-val. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Beta-val. Each strength is a separate product. May repeat for multiple part products. Format is nnn.

Therapeutic Equivalence (TE) Code - AB
The TE Code indicates the therapeutic equivalence rating of generic to innovator Rx products.

Approval Date - Dec 19, 1985
The date Beta-val 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 Beta-val. 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 Beta-val is in. Format is RX, OTC, DISCN.

Applicant Full Name - Teva Pharmaceuticals Usa Inc
The full name of the firm holding legal responsibility for the new application of Beta-val.

Beta-val