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LopressorDrug - Lopressor The trade name of the product as shown on the labeling.
Dosage -
TABLET; ORAL
Active Ingredient(s) -
Metoprolol Tartrate
Strength -
100MG
Applicant -
NOVARTIS
New Drug Application (NDA) Number -
017963
Product Number -
002
Therapeutic Equivalence (TE) Code -
AB
Approval Date -
Approved Prior to Jan 1, 1982
Reference Listed Drug (RLD) -
No
Type -
RX
Applicant Full Name -
Novartis Pharmaceuticals Corp
Lopressor
Metoprolol Tartrate 1mg/ml Injectable; Injection
Metoprolol Tartrate 1mg/ml Injectable; Injection Metoprolol Tartrate 1mg/ml Injectable; Injection Metoprolol Tartrate 1mg/ml Injectable; Injection Lopressor 100mg Tablet; Oral Toprol-xl Eq 100mg Tartrate Tablet, Extended Release; Oral Toprol-xl Eq 200mg Tartrate Tablet, Extended Release; Oral Toprol-xl Eq 25mg Tartrate Tablet, Extended Release; Oral Toprol-xl Eq 50mg Tartrate Tablet, Extended Release; Oral Lopressor 1mg/ml Injectable; Injection NewDrugInformation |