Search by Drug Name or NDC
NDC 69097-0856-15 Fosinopril Sodium 10 mg/1 Details
Fosinopril Sodium 10 mg/1
Fosinopril Sodium is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Cipla USA Inc.. The primary component is FOSINOPRIL SODIUM.
MedlinePlus Drug Summary
Fosinopril is used alone or in combination with other medications to treat high blood pressure. It is also used in combination with other medications to treat heart failure. Fosinopril is in a class of medications called angiotensin-converting enzyme (ACE) inhibitors. It works by decreasing certain chemicals that tighten the blood vessels, so blood flows more smoothly and the heart can pump blood more efficiently. High blood pressure is a common condition and when not treated, can cause damage to the brain, heart, blood vessels, kidneys and other parts of the body. Damage to these organs may cause heart disease, a heart attack, heart failure, stroke, kidney failure, loss of vision, and other problems. In addition to taking medication, making lifestyle changes will also help to control your blood pressure. These changes include eating a diet that is low in fat and salt, maintaining a healthy weight, exercising at least 30 minutes most days, not smoking, and using alcohol in moderation.
Related Packages: 69097-0856-15Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Fosinopril
Product Information
| NDC | 69097-0856 |
|---|---|
| Product ID | 69097-856_6d672087-9b6a-4afe-8c3e-0616943a82cf |
| Associated GPIs | 36100027100310 |
| GCN Sequence Number | 016017 |
| GCN Sequence Number Description | fosinopril sodium TABLET 10 MG ORAL |
| HIC3 | A4D |
| HIC3 Description | ANTIHYPERTENSIVES, ACE INHIBITORS |
| GCN | 48581 |
| HICL Sequence Number | 006106 |
| HICL Sequence Number Description | FOSINOPRIL SODIUM |
| Brand/Generic | Generic |
| Proprietary Name | Fosinopril Sodium |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Fosinopril |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 10 |
| Active Ingredient Units | mg/1 |
| Substance Name | FOSINOPRIL SODIUM |
| Labeler Name | Cipla USA Inc. |
| Pharmaceutical Class | Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA077222 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 69097-0856-15 (69097085615)
| NDC Package Code | 69097-856-15 |
|---|---|
| Billing NDC | 69097085615 |
| Package | 1000 TABLET in 1 BOTTLE (69097-856-15) |
| Marketing Start Date | 2016-06-16 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |