Details for New Drug Application (NDA): 207807
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The generic ingredient in AMLODIPINE AND OLMESARTAN MEDOXOMIL is amlodipine besylate; olmesartan medoxomil. There are fifty drug master file entries for this compound. Eighteen suppliers are listed for this compound. Additional details are available on the amlodipine besylate; olmesartan medoxomil profile page.
Summary for 207807
Tradename: | AMLODIPINE AND OLMESARTAN MEDOXOMIL |
Applicant: | Glenmark Pharms Ltd |
Ingredient: | amlodipine besylate; olmesartan medoxomil |
Patents: | 0 |
Suppliers and Packaging for NDA: 207807
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
AMLODIPINE AND OLMESARTAN MEDOXOMIL | amlodipine besylate; olmesartan medoxomil | TABLET;ORAL | 207807 | ANDA | medsource pharmaceuticals | 45865-923 | 45865-923-30 | 30 TABLET, FILM COATED in 1 BOTTLE (45865-923-30) |
AMLODIPINE AND OLMESARTAN MEDOXOMIL | amlodipine besylate; olmesartan medoxomil | TABLET;ORAL | 207807 | ANDA | medsource pharmaceuticals | 45865-935 | 45865-935-30 | 30 TABLET, FILM COATED in 1 BOTTLE (45865-935-30) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | EQ 5MG BASE;20MG | ||||
Approval Date: | Jul 5, 2017 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | EQ 5MG BASE;40MG | ||||
Approval Date: | Jul 5, 2017 | TE: | AB | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | EQ 10MG BASE;20MG | ||||
Approval Date: | Jul 5, 2017 | TE: | AB | RLD: | No |
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