Details for New Drug Application (NDA): 073665
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The generic ingredient in ATENOLOL AND CHLORTHALIDONE is atenolol; chlorthalidone. There are thirty-four drug master file entries for this compound. Eleven suppliers are listed for this compound. Additional details are available on the atenolol; chlorthalidone profile page.
Summary for 073665
Tradename: | ATENOLOL AND CHLORTHALIDONE |
Applicant: | Watson Labs |
Ingredient: | atenolol; chlorthalidone |
Patents: | 0 |
Pharmacology for NDA: 073665
Mechanism of Action | Adrenergic beta-Antagonists |
Physiological Effect | Increased Diuresis |
Suppliers and Packaging for NDA: 073665
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
ATENOLOL AND CHLORTHALIDONE | atenolol; chlorthalidone | TABLET;ORAL | 073665 | ANDA | Actavis Pharma, Inc. | 0591-5782 | 0591-5782-01 | 100 TABLET in 1 BOTTLE (0591-5782-01) |
ATENOLOL AND CHLORTHALIDONE | atenolol; chlorthalidone | TABLET;ORAL | 073665 | ANDA | Actavis Pharma, Inc. | 0591-5783 | 0591-5783-01 | 100 TABLET in 1 BOTTLE (0591-5783-01) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 50MG;25MG | ||||
Approval Date: | Jul 2, 1992 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 100MG;25MG | ||||
Approval Date: | Jul 2, 1992 | TE: | AB | RLD: | No |
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