Carteolol Hcl
Drug - Carteolol 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) -
Carteolol Hydrochloride
Multiple ingredients are in alphabetical order.
Strength -
1%
The potency of the active ingredient(s), Carteolol Hydrochloride. May repeat for multiple part products.
Applicant -
ALCON
The firm name holding legal responsibility for Carteolol Hcl. The firm name is condensed to a maximum twenty character unique string.
New Drug Application (NDA) Number -
075476
The FDA assigned number to Carteolol Hcl. Format is nnnnnn.
Product Number -
001
The FDA assigned number to identify Carteolol 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 -
Jan 3, 2000
The date Carteolol 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 Carteolol 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 Carteolol Hcl is in. Format is RX, OTC, DISCN.
Applicant Full Name -
Alcon Laboratories Inc
The full name of the firm holding legal responsibility for the new application of Carteolol Hcl.
Carteolol Hcl
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