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MoviPrep
MoviPrep - 65649-201-75 - (POLYETHYLENE GLYCOL 3350, SODIUM SULFATE, SODIUM CHLORIDE, POTASSIUM CHLORIDE, ASCORBIC ACID, SODIUM ASCORBATE)
Drug Information of MoviPrep
| Product NDC: | 65649-201 |
| Proprietary Name: | MoviPrep |
| Non Proprietary Name: | POLYETHYLENE GLYCOL 3350, SODIUM SULFATE, SODIUM CHLORIDE, POTASSIUM CHLORIDE, ASCORBIC ACID, SODIUM ASCORBATE |
| Active Ingredient(s): | & nbsp; POLYETHYLENE GLYCOL 3350, SODIUM SULFATE, SODIUM CHLORIDE, POTASSIUM CHLORIDE, ASCORBIC ACID, SODIUM ASCORBATE |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of MoviPrep
| Product NDC: | 65649-201 |
| Labeler Name: | Salix Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021881 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20061001 |
Package Information of MoviPrep
| Package NDC: | 65649-201-75 |
| Package Description: | 1 KIT in 1 CONTAINER (65649-201-75) * 1 L in 1 POUCH * 1 L in 1 POUCH |
NDC Information of MoviPrep
| NDC Code | 65649-201-75 |
| Proprietary Name | MoviPrep |
| Package Description | 1 KIT in 1 CONTAINER (65649-201-75) * 1 L in 1 POUCH * 1 L in 1 POUCH |
| Product NDC | 65649-201 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | POLYETHYLENE GLYCOL 3350, SODIUM SULFATE, SODIUM CHLORIDE, POTASSIUM CHLORIDE, ASCORBIC ACID, SODIUM ASCORBATE |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20061001 |
| Marketing Category Name | NDA |
| Labeler Name | Salix Pharmaceuticals, Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
