Dipivefrin Hcl

   
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Dipivefrin Hcl


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

Dosage - SOLUTION/DROPS; OPHTHALMIC
The product dosage form and route separated by a semi-colon.

Active Ingredient(s) - Dipivefrin Hydrochloride
Multiple ingredients are in alphabetical order.

Strength - 0.1%
The potency of the active ingredient(s), Dipivefrin Hydrochloride. May repeat for multiple part products.

Applicant - BAUSCH AND LOMB
The firm name holding legal responsibility for Dipivefrin Hcl. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 074188
The FDA assigned number to Dipivefrin Hcl. Format is nnnnnn.

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

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

Approval Date - May 19, 1995
The date Dipivefrin Hcl 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 Dipivefrin Hcl. 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 Dipivefrin Hcl is in. Format is RX, OTC, DISCN.

Applicant Full Name - Bausch And Lomb Pharmaceuticals Inc
The full name of the firm holding legal responsibility for the new application of Dipivefrin Hcl.

Dipivefrin Hcl