NDC Code | 0051-1543-05 |
Package Description | 5 BLISTER PACK in 1 TRAY (0051-1543-05) > 3 TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE in 1 BLISTER PACK |
Product NDC | 0051-1543 |
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 | 20200831 |
Marketing Category Name | APPROVED DRUG PRODUCT MANUFACTURED UNDER CONTRACT |
Application Number | NDA021428 |
Manufacturer | AbbVie Inc. |
Substance Name | LANSOPRAZOLE |
Strength | 15 |
Strength Unit | mg/1 |
Pharmacy Classes | Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA],Inhibition Gastric Acid Secretion [PE] |