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NDC 42291-0619-01 MINOXIDIL 10 mg/1 Details
MINOXIDIL 10 mg/1
MINOXIDIL is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by AvKARE. The primary component is MINOXIDIL.
MedlinePlus Drug Summary
Minoxidil is used with other medications to treat high blood pressure. It is in a class of medications called vasodilators. It works by relaxing the blood vessels so that blood can flow more easily through the body. 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: 42291-0619-01Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Minoxidil
Product Information
| NDC | 42291-0619 |
|---|---|
| Product ID | 42291-619_089f9ac0-43ca-f649-e063-6294a90a76b9 |
| Associated GPIs | 36400020000310 |
| GCN Sequence Number | 000299 |
| GCN Sequence Number Description | minoxidil TABLET 10 MG ORAL |
| HIC3 | A4A |
| HIC3 Description | ANTIHYPERTENSIVES, VASODILATORS |
| GCN | 01290 |
| HICL Sequence Number | 000093 |
| HICL Sequence Number Description | MINOXIDIL |
| Brand/Generic | Generic |
| Proprietary Name | MINOXIDIL |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | minoxidil |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 10 |
| Active Ingredient Units | mg/1 |
| Substance Name | MINOXIDIL |
| Labeler Name | AvKARE |
| Pharmaceutical Class | Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA072709 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 42291-0619-01 (42291061901)
| NDC Package Code | 42291-619-01 |
|---|---|
| Billing NDC | 42291061901 |
| Package | 100 TABLET in 1 BOTTLE (42291-619-01) |
| Marketing Start Date | 2013-08-01 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |