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 |