| NDC Code | 43063-127-60 | 
|---|
			| Package Description | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-127-60) | 
|---|
			| Product NDC | 43063-127 | 
|---|
			| Product Type Name | HUMAN PRESCRIPTION DRUG | 
|---|
			| Proprietary Name | Carvedilol | 
|---|
			
			| Non-Proprietary Name | Carvedilol | 
|---|
			| Dosage Form | TABLET, FILM COATED | 
|---|
			| Usage | ORAL | 
|---|
			| Start Marketing Date | 20090323 | 
|---|
			
			| Marketing Category Name | ANDA | 
|---|
			| Application Number | ANDA078332 | 
|---|
			| Manufacturer | PD-Rx Pharmaceuticals, Inc. | 
|---|
			| Substance Name | CARVEDILOL | 
|---|
			| Strength | 6.25 | 
|---|
			| Strength Unit | mg/1 | 
|---|
			| Pharmacy Classes | Adrenergic alpha-Antagonists [MoA],Adrenergic beta1-Antagonists [MoA],Adrenergic beta2-Antagonists [MoA],alpha-Adrenergic Blocker [EPC],beta-Adrenergic Blocker [EPC] | 
|---|