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PREVPAC
PREVPAC - 64764-702-00 - (lansoprazole, amoxicillin and clarithromycin)
Drug Information of PREVPAC
| Product NDC: | 64764-702 |
| Proprietary Name: | PREVPAC |
| Non Proprietary Name: | lansoprazole, amoxicillin and clarithromycin |
| Active Ingredient(s): | & nbsp; lansoprazole, amoxicillin and clarithromycin |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PREVPAC
| Product NDC: | 64764-702 |
| Labeler Name: | Takeda Pharmaceuticals America, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050757 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19971202 |
Package Information of PREVPAC
| Package NDC: | 64764-702-00 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (64764-702-00) > 1 KIT in 1 BLISTER PACK |
NDC Information of PREVPAC
| NDC Code | 64764-702-00 |
| Proprietary Name | PREVPAC |
| Package Description | 1 BLISTER PACK in 1 CARTON (64764-702-00) > 1 KIT in 1 BLISTER PACK |
| Product NDC | 64764-702 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | lansoprazole, amoxicillin and clarithromycin |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 19971202 |
| Marketing Category Name | NDA |
| Labeler Name | Takeda Pharmaceuticals America, Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
