| NDC Code | 68071-3019-7 |
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| Package Description | 7 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68071-3019-7) |
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| Product NDC | 68071-3019 |
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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 | CAPSULE, DELAYED RELEASE PELLETS |
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| Usage | ORAL |
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| Start Marketing Date | 20130823 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA202366 |
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| Manufacturer | NuCare Pharmaceuticals, 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 | Inhibition Gastric Acid Secretion [PE], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA] |
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