Amlobenz is a Oral Capsule in the Human Prescription Drug category. It is labeled and distributed by Rebel Distributors Corp. The primary component is Amlodipine Besylate; Benazepril Hydrochloride.
| Product ID | 21695-866_241e7477-ecae-4f84-8410-bbfaa9f57ed0 |
| NDC | 21695-866 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Amlobenz |
| Generic Name | Amlobenz |
| Dosage Form | Capsule |
| Route of Administration | ORAL |
| Marketing Start Date | 2010-04-19 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA077183 |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE |
| Active Ingredient Strength | 5 mg/1; mg/1 |
| Pharm Classes | Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS],Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE] |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
| Marketing Start Date | 2010-04-19 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA077183 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-04-19 |
| Inactivation Date | 2019-09-24 |
| Ingredient | Strength |
|---|---|
| AMLODIPINE BESYLATE | 5 mg/1 |
| SPL SET ID: | 241e7477-ecae-4f84-8410-bbfaa9f57ed0 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 21695-866 | Amlobenz | Amlobenz |
| 21695-916 | Amlobenz | Amlobenz |