| NDC Code | 0051-1544-13 |
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| Package Description | 10 BLISTER PACK in 1 CARTON (0051-1544-13) > 10 TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE in 1 BLISTER PACK |
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| Product NDC | 0051-1544 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Lansoprazole |
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| Non-Proprietary Name | Lansoprazole |
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| Dosage Form | TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20020830 |
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| End Marketing Date | 20201130 |
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| Marketing Category Name | APPROVED DRUG PRODUCT MANUFACTURED UNDER CONTRACT |
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| Application Number | NDA021428 |
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| Manufacturer | AbbVie Inc. |
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| Substance Name | LANSOPRAZOLE |
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| Strength | 30 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA],Inhibition Gastric Acid Secretion [PE] |
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