| NDC Code | 55111-363-05 | 
|---|
			| Package Description | 500 CAPSULE in 1 BOTTLE (55111-363-05) | 
|---|
			| Product NDC | 55111-363 | 
|---|
			| Product Type Name | HUMAN PRESCRIPTION DRUG | 
|---|
			| Proprietary Name | Omeprazole And Sodium Bicrabonate | 
|---|
			
			| Non-Proprietary Name | Omeprazole And Sodium Bicrabonate | 
|---|
			| Dosage Form | CAPSULE | 
|---|
			| Usage | ORAL | 
|---|
			| Start Marketing Date | 20160715 | 
|---|
			| End Marketing Date | 20240731 | 
|---|
			| Marketing Category Name | ANDA | 
|---|
			| Application Number | ANDA204068 | 
|---|
			| Manufacturer | Dr.Reddy's Laboratories Limited | 
|---|
			| Substance Name | OMEPRAZOLE; SODIUM BICARBONATE | 
|---|
			| Strength | 20; 1100 | 
|---|
			| Strength Unit | mg/1; mg/1 | 
|---|
			| Pharmacy Classes | Alkalinizing Activity [MoA], Cytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA] | 
|---|