| NDC Code | 43598-561-78 |
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| Package Description | 100 BLISTER PACK in 1 CARTON (43598-561-78) / 10 TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE in 1 BLISTER PACK (43598-561-79) |
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| Product NDC | 43598-561 |
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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 | 20210201 |
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| End Marketing Date | 20260930 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA210465 |
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| Manufacturer | Dr.Reddys Laboratories 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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