| NDC Code | 0051-1544-05 | 
|---|
			| Package Description | 5 BLISTER PACK in 1 TRAY (0051-1544-05)  > 3 TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE in 1 BLISTER PACK | 
|---|
			| Product NDC | 0051-1544 | 
|---|
			| Product Type Name | HUMAN PRESCRIPTION DRUG | 
|---|
			| Proprietary Name | Lansoprazole | 
|---|
			
			| Non-Proprietary Name | Lansoprazole | 
|---|
			| Dosage Form | TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE | 
|---|
			| Usage | ORAL | 
|---|
			| Start Marketing Date | 20020830 | 
|---|
			| End Marketing Date | 20201130 | 
|---|
			| Marketing Category Name | APPROVED DRUG PRODUCT MANUFACTURED UNDER CONTRACT | 
|---|
			| Application Number | NDA021428 | 
|---|
			| Manufacturer | AbbVie Inc. | 
|---|
			| Substance Name | LANSOPRAZOLE | 
|---|
			| Strength | 30 | 
|---|
			| Strength Unit | mg/1 | 
|---|
			| Pharmacy Classes | Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA],Inhibition Gastric Acid Secretion [PE] | 
|---|