Details for New Drug Application (NDA): 077900
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The generic ingredient in RAMIPRIL is ramipril. There are nineteen drug master file entries for this compound. Nineteen suppliers are listed for this compound. Additional details are available on the ramipril profile page.
Pharmacology for NDA: 077900
Mechanism of Action | Angiotensin-converting Enzyme Inhibitors |
Medical Subject Heading (MeSH) Categories for 077900
Suppliers and Packaging for NDA: 077900
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
RAMIPRIL | ramipril | CAPSULE;ORAL | 077900 | ANDA | Hikma Pharmaceuticals USA Inc. | 0054-0106 | 0054-0106-25 | 100 CAPSULE in 1 BOTTLE (0054-0106-25) |
RAMIPRIL | ramipril | CAPSULE;ORAL | 077900 | ANDA | Hikma Pharmaceuticals USA Inc. | 0054-0107 | 0054-0107-20 | 10 BLISTER PACK in 1 CARTON (0054-0107-20) / 10 CAPSULE in 1 BLISTER PACK |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | 1.25MG | ||||
Approval Date: | Jun 18, 2008 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | 2.5MG | ||||
Approval Date: | Jun 18, 2008 | TE: | AB | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | 5MG | ||||
Approval Date: | Jun 18, 2008 | TE: | AB | RLD: | No |
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