Details for New Drug Application (NDA): 200981
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The generic ingredient in METOPROLOL TARTRATE is hydrochlorothiazide; metoprolol tartrate. There are thirty-two drug master file entries for this compound. Five suppliers are listed for this compound. Additional details are available on the hydrochlorothiazide; metoprolol tartrate profile page.
Summary for 200981
Tradename: | METOPROLOL TARTRATE |
Applicant: | Rubicon |
Ingredient: | metoprolol tartrate |
Patents: | 0 |
Pharmacology for NDA: 200981
Mechanism of Action | Adrenergic beta-Antagonists |
Suppliers and Packaging for NDA: 200981
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
METOPROLOL TARTRATE | metoprolol tartrate | TABLET;ORAL | 200981 | ANDA | A-S Medication Solutions | 50090-6083 | 50090-6083-0 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-6083-0) |
METOPROLOL TARTRATE | metoprolol tartrate | TABLET;ORAL | 200981 | ANDA | A-S Medication Solutions | 50090-6083 | 50090-6083-1 | 60 TABLET, FILM COATED in 1 BOTTLE (50090-6083-1) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 25MG | ||||
Approval Date: | Oct 28, 2014 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 50MG | ||||
Approval Date: | Oct 28, 2014 | TE: | AB | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 100MG | ||||
Approval Date: | Oct 28, 2014 | TE: | AB | RLD: | No |
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