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Fosinopril Sodium And HydrochlorothiazideDrug - Fosinopril Sodium And Hydrochlorothiazide The trade name of the product as shown on the labeling.
Dosage -
TABLET; ORAL
Active Ingredient(s) -
Fosinopril Sodium; Hydrochlorothiazide
Strength -
10MG;12.5MG
Applicant -
WATSON LABS
New Drug Application (NDA) Number -
077144
Product Number -
001
Therapeutic Equivalence (TE) Code -
AB
Approval Date -
Aug 16, 2005
Reference Listed Drug (RLD) -
No
Type -
RX
Applicant Full Name -
Watson Laboratories Inc
Fosinopril Sodium And Hydrochlorothiazide
Fosinopril Sodium And Hydrochlorothiazide 10mg;12.5mg Tablet; Oral
Fosinopril Sodium And Hydrochlorothiazide 20mg;12.5mg Tablet; Oral Fosinopril Sodium And Hydrochlorothiazide 10mg;12.5mg Tablet; Oral Fosinopril Sodium And Hydrochlorothiazide 20mg;12.5mg Tablet; Oral Fosinopril Sodium And Hydrochlorothiazide 10mg;12.5mg Tablet; Oral Monopril 10mg Tablet; Oral Monopril 20mg Tablet; Oral Monopril 40mg Tablet; Oral Fosinopril Sodium And Hydrochlorothiazide 10mg;12.5mg Tablet; Oral Fosinopril Sodium And Hydrochlorothiazide 20mg;12.5mg Tablet; Oral NewDrugInformation |