Lotensin is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Validus Pharmaceuticals Llc. The primary component is Benazepril Hydrochloride.
| Product ID | 30698-448_01747b79-4170-4696-9a85-23fd8aa04ecf |
| NDC | 30698-448 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Lotensin |
| Generic Name | Benazepril Hydrochloride |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 1991-06-21 |
| Marketing Category | NDA / NDA |
| Application Number | NDA019851 |
| Labeler Name | Validus Pharmaceuticals LLC |
| Substance Name | BENAZEPRIL HYDROCHLORIDE |
| Active Ingredient Strength | 10 mg/1 |
| Pharm Classes | Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |
| Marketing Start Date | 1991-06-21 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | NDA |
| Application Number | NDA019851 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1991-06-21 |
| Ingredient | Strength |
|---|---|
| BENAZEPRIL HYDROCHLORIDE | 10 mg/1 |
| SPL SET ID: | 2abb091b-a53e-46b0-9b84-e5ee8f2bdd8e |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 30698-448 | Lotensin | benazepril hydrochloride |
| 30698-449 | Lotensin | benazepril hydrochloride |
| 30698-450 | Lotensin | benazepril hydrochloride |
| 0185-0053 | Benazepril Hydrochloride | Benazepril Hydrochloride |
| 0185-0505 | Benazepril Hydrochloride | Benazepril Hydrochloride |
| 0185-0820 | Benazepril Hydrochloride | Benazepril Hydrochloride |
| 0378-0441 | Benazepril Hydrochloride | benazepril hydrochloride |
| 0378-0443 | Benazepril Hydrochloride | benazepril hydrochloride |
| 0378-0444 | Benazepril Hydrochloride | benazepril hydrochloride |
| 0378-0447 | Benazepril Hydrochloride | benazepril hydrochloride |
| 10544-554 | Benazepril Hydrochloride | Benazepril Hydrochloride |
| 10544-561 | Benazepril Hydrochloride | Benazepril Hydrochloride |
| 10544-566 | Benazepril Hydrochloride | Benazepril Hydrochloride |
| 13811-627 | benazepril hydrochloride | Benazepril hydrochloride |
| 13811-628 | BENAZEPRIL HYDROCHLORIDE | Benazepril hydrochloride |
| 13811-629 | BENAZEPRIL HYDROCHLORIDE | Benazepril hydrochloride |
| 13811-630 | BENAZEPRIL HYDROCHLORIDE | Benazepril hydrochloride |
| 21695-326 | Benazepril Hydrochloride | Benazepril Hydrochloride |
| 21695-327 | Benazepril Hydrochloride | Benazepril Hydrochloride |
| 21695-612 | Benazepril Hydrochloride | Benazepril Hydrochloride |
| 21695-877 | Benazepril Hydrochloride | Benazepril Hydrochloride |
| 23155-749 | Benazepril Hydrochloride | Benazepril Hydrochloride |
| 23155-750 | Benazepril Hydrochloride | Benazepril Hydrochloride |
| 23155-751 | Benazepril Hydrochloride | Benazepril Hydrochloride |
| 23155-752 | Benazepril Hydrochloride | Benazepril Hydrochloride |
| 33261-179 | Benazepril Hydrochloride | Benazepril Hydrochloride |
| 33261-180 | Benazepril Hydrochloride | Benazepril Hydrochloride |
| 33261-846 | Benazepril Hydrochloride | Benazepril Hydrochloride |
| 42291-160 | Benazepril Hydrochloride | Benazepril Hydrochloride |
| 42291-161 | Benazepril Hydrochloride | Benazepril Hydrochloride |
| 42291-162 | Benazepril Hydrochloride | Benazepril Hydrochloride |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() LOTENSIN 74108632 1692378 Dead/Cancelled |
CIBA-GEIGY CORPORATION 1990-10-24 |
![]() LOTENSIN 73783376 1599155 Live/Registered |
CIBA-GEIGY CORPORATION 1989-02-27 |