Details for New Drug Application (NDA): 203281
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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 203281
| Tradename: | OLMESARTAN MEDOXOMIL |
| Applicant: | Glenmark Pharms Ltd |
| Ingredient: | olmesartan medoxomil |
| Patents: | 0 |
Pharmacology for NDA: 203281
| Mechanism of Action | Angiotensin 2 Receptor Antagonists |
Medical Subject Heading (MeSH) Categories for 203281
Suppliers and Packaging for NDA: 203281
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| OLMESARTAN MEDOXOMIL | olmesartan medoxomil | TABLET;ORAL | 203281 | ANDA | A-S Medication Solutions | 50090-6686 | 50090-6686-0 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-6686-0) |
| OLMESARTAN MEDOXOMIL | olmesartan medoxomil | TABLET;ORAL | 203281 | ANDA | Glenmark Pharmaceuticals Inc., USA | 68462-436 | 68462-436-10 | 1000 TABLET, FILM COATED in 1 BOTTLE (68462-436-10) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 5MG | ||||
| Approval Date: | May 25, 2017 | TE: | AB | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 20MG | ||||
| Approval Date: | May 25, 2017 | TE: | AB | RLD: | No | ||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 40MG | ||||
| Approval Date: | May 25, 2017 | TE: | AB | RLD: | No | ||||
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