Details for New Drug Application (NDA): 210682
✉ Email this page to a colleague
The generic ingredient in OLMESARTAN MEDOXOMIL is amlodipine besylate; hydrochlorothiazide; olmesartan medoxomil. There are fifty drug master file entries for this compound. Seven suppliers are listed for this compound. Additional details are available on the amlodipine besylate; hydrochlorothiazide; olmesartan medoxomil profile page.
Summary for 210682
| Tradename: | OLMESARTAN MEDOXOMIL |
| Applicant: | Cadila Pharms Ltd |
| Ingredient: | olmesartan medoxomil |
| Patents: | 0 |
Pharmacology for NDA: 210682
| Mechanism of Action | Angiotensin 2 Receptor Antagonists |
Medical Subject Heading (MeSH) Categories for 210682
Suppliers and Packaging for NDA: 210682
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| OLMESARTAN MEDOXOMIL | olmesartan medoxomil | TABLET;ORAL | 210682 | ANDA | Cadila Pharmaceuticals Limited | 71209-079 | 71209-079-01 | 30 TABLET, COATED in 1 BOTTLE (71209-079-01) |
| OLMESARTAN MEDOXOMIL | olmesartan medoxomil | TABLET;ORAL | 210682 | ANDA | Cadila Pharmaceuticals Limited | 71209-079 | 71209-079-04 | 90 TABLET, COATED in 1 BOTTLE (71209-079-04) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 5MG | ||||
| Approval Date: | Nov 8, 2024 | TE: | AB | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 20MG | ||||
| Approval Date: | Nov 8, 2024 | TE: | AB | RLD: | No | ||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 40MG | ||||
| Approval Date: | Nov 8, 2024 | TE: | AB | RLD: | No | ||||
Complete Access Available with Subscription
