| NDC Code | 49884-172-11 |
|---|
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (49884-172-11) |
|---|
| Product NDC | 49884-172 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Amlodipine, Valsartan, Hydrochlorothiazide |
|---|
| Non-Proprietary Name | Amlodipine Besylate Valsartan Hydrochlorothiazide |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20150601 |
|---|
| End Marketing Date | 20220531 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA201087 |
|---|
| Manufacturer | Par Pharmaceutical, Inc. |
|---|
| Substance Name | AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; VALSARTAN |
|---|
| Strength | 5; 12.5; 160 |
|---|
| Strength Unit | mg/1; mg/1; mg/1 |
|---|
| Pharmacy Classes | Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Calcium Channel Antagonists [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS] |
|---|