Details for New Drug Application (NDA): 077877
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The generic ingredient in ATENOLOL 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 077877
Tradename: | ATENOLOL |
Applicant: | Ipca Labs Ltd |
Ingredient: | atenolol |
Patents: | 0 |
Pharmacology for NDA: 077877
Mechanism of Action | Adrenergic beta-Antagonists |
Medical Subject Heading (MeSH) Categories for 077877
Suppliers and Packaging for NDA: 077877
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
ATENOLOL | atenolol | TABLET;ORAL | 077877 | ANDA | Proficient Rx LP | 63187-092 | 63187-092-30 | 30 TABLET in 1 BOTTLE (63187-092-30) |
ATENOLOL | atenolol | TABLET;ORAL | 077877 | ANDA | Proficient Rx LP | 63187-092 | 63187-092-90 | 90 TABLET in 1 BOTTLE (63187-092-90) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 25MG | ||||
Approval Date: | Dec 27, 2006 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 50MG | ||||
Approval Date: | Dec 27, 2006 | TE: | AB | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 100MG | ||||
Approval Date: | Dec 27, 2006 | TE: | AB | RLD: | No |
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