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NDC 70710-1179-01 Ambrisentan 5 mg/1 Details
Ambrisentan 5 mg/1
Ambrisentan is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Zydus Pharmaceuticals USA Inc.. The primary component is AMBRISENTAN.
MedlinePlus Drug Summary
Ambrisentan is used alone or in combination with tadalafil (Adcirca, Cialis) to treat pulmonary arterial hypertension (PAH, high blood pressure in the vessels that carry blood to the lungs). Ambrisentan may improve the ability to exercise and slow the worsening of symptoms in people with PAH. Ambrisentan is in a class of medications called endothelin receptor antagonists. It works by stopping the action of endothelin, a natural substance that causes blood vessels to narrow and prevents normal blood flow in people who have PAH.
Related Packages: 70710-1179-01Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Ambrisentan
Product Information
| NDC | 70710-1179 |
|---|---|
| Product ID | 70710-1179_bbe506db-b0b4-4ef0-9686-ab0b8d52c39d |
| Associated GPIs | 40160007000310 |
| GCN Sequence Number | 062792 |
| GCN Sequence Number Description | ambrisentan TABLET 5 MG ORAL |
| HIC3 | B1B |
| HIC3 Description | PULMONARY ANTI-HTN, ENDOTHELIN RECEPTOR ANTAGONIST |
| GCN | 98566 |
| HICL Sequence Number | 034849 |
| HICL Sequence Number Description | AMBRISENTAN |
| Brand/Generic | Generic |
| Proprietary Name | Ambrisentan |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Ambrisentan |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET, FILM COATED |
| Route | ORAL |
| Active Ingredient Strength | 5 |
| Active Ingredient Units | mg/1 |
| Substance Name | AMBRISENTAN |
| Labeler Name | Zydus Pharmaceuticals USA Inc. |
| Pharmaceutical Class | Endothelin Receptor Antagonist [EPC], Endothelin Receptor Antagonists [MoA] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA210058 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 70710-1179-01 (70710117901)
| NDC Package Code | 70710-1179-1 |
|---|---|
| Billing NDC | 70710117901 |
| Package | 100 TABLET, FILM COATED in 1 BOTTLE (70710-1179-1) |
| Marketing Start Date | 2019-04-12 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |