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Prevacid
Prevacid - 64764-541-05 - (lansoprazole)
Drug Information of Prevacid
| Product NDC: | 64764-541 |
| Proprietary Name: | Prevacid |
| Non Proprietary Name: | lansoprazole |
| Active Ingredient(s): | 15 mg/1 & nbsp; lansoprazole |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, DELAYED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Prevacid
| Product NDC: | 64764-541 |
| Labeler Name: | Takeda Pharmaceuticals America, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020406 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19950510 |
Package Information of Prevacid
| Package NDC: | 64764-541-05 |
| Package Description: | 5 BLISTER PACK in 1 TRAY (64764-541-05) > 4 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK |
NDC Information of Prevacid
| NDC Code | 64764-541-05 |
| Proprietary Name | Prevacid |
| Package Description | 5 BLISTER PACK in 1 TRAY (64764-541-05) > 4 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK |
| Product NDC | 64764-541 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | lansoprazole |
| Dosage Form Name | CAPSULE, DELAYED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 19950510 |
| Marketing Category Name | NDA |
| Labeler Name | Takeda Pharmaceuticals America, Inc. |
| Substance Name | LANSOPRAZOLE |
| Strength Number | 15 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA] |
