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OcupressDrug - Ocupress The trade name of the product as shown on the labeling.
Dosage -
SOLUTION/DROPS; OPHTHALMIC
Active Ingredient(s) -
Carteolol Hydrochloride
Strength -
1%
Applicant -
NOVARTIS
New Drug Application (NDA) Number -
019972
Product Number -
001
Therapeutic Equivalence (TE) Code -
AT
Approval Date -
May 23, 1990
Reference Listed Drug (RLD) -
Yes
Type -
RX
Applicant Full Name -
Novartis Pharmaceuticals Corp
Ocupress
Carteolol Hcl 1% Solution/drops; Ophthalmic
Ocupress 1% Solution/drops; Ophthalmic Proketazine 50mg/ml Concentrate; Oral Proketazine 12.5mg Tablet; Oral Proketazine 25mg Tablet; Oral Proketazine 50mg Tablet; Oral Rimadyl 100mg Tablet; Oral Rimadyl 150mg Tablet; Oral Carteolol Hcl 1% Solution/drops; Ophthalmic Carteolol Hcl 1% Solution/drops; Ophthalmic NewDrugInformation |