| NDC Code | 0054-0547-18 | 
|---|
			| Package Description | 3 BLISTER PACK in 1 CARTON (0054-0547-18)  > 10 TABLET in 1 BLISTER PACK | 
|---|
			| Product NDC | 0054-0547 | 
|---|
			| Product Type Name | HUMAN PRESCRIPTION DRUG | 
|---|
			| Proprietary Name | Telmisartan And Hydrochlorothiazide | 
|---|
			
			| Non-Proprietary Name | Telmisartan And Hydrochlorothiazide | 
|---|
			| Dosage Form | TABLET | 
|---|
			| Usage | ORAL | 
|---|
			| Start Marketing Date | 20140228 | 
|---|
			| End Marketing Date | 20221130 | 
|---|
			| Marketing Category Name | NDA AUTHORIZED GENERIC | 
|---|
			| Application Number | NDA021162 | 
|---|
			| Manufacturer | Hikma Pharmaceuticals USA Inc. | 
|---|
			| Substance Name | HYDROCHLOROTHIAZIDE; TELMISARTAN | 
|---|
			| Strength | 25; 80 | 
|---|
			| Strength Unit | mg/1; mg/1 | 
|---|
			| Pharmacy Classes | Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS] | 
|---|