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MOVIPREP
MOVIPREP - 54868-5890-0 - (POLYETHYLENE GLYCOL 3350, SODIUM SULFATE, SODIUM CHLORIDE, POTASSIUM CHLORIDE, SODIUM ASCORBATE and ASCORBIC ACID)
Drug Information of MOVIPREP
| Product NDC: | 54868-5890 |
| Proprietary Name: | MOVIPREP |
| Non Proprietary Name: | POLYETHYLENE GLYCOL 3350, SODIUM SULFATE, SODIUM CHLORIDE, POTASSIUM CHLORIDE, SODIUM ASCORBATE and ASCORBIC ACID |
| Active Ingredient(s): | & nbsp; POLYETHYLENE GLYCOL 3350, SODIUM SULFATE, SODIUM CHLORIDE, POTASSIUM CHLORIDE, SODIUM ASCORBATE and ASCORBIC ACID |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of MOVIPREP
| Product NDC: | 54868-5890 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021881 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20080530 |
Package Information of MOVIPREP
| Package NDC: | 54868-5890-0 |
| Package Description: | 1 KIT in 1 CONTAINER (54868-5890-0) * 1 L in 1 POUCH * 1 L in 1 POUCH |
NDC Information of MOVIPREP
| NDC Code | 54868-5890-0 |
| Proprietary Name | MOVIPREP |
| Package Description | 1 KIT in 1 CONTAINER (54868-5890-0) * 1 L in 1 POUCH * 1 L in 1 POUCH |
| Product NDC | 54868-5890 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | POLYETHYLENE GLYCOL 3350, SODIUM SULFATE, SODIUM CHLORIDE, POTASSIUM CHLORIDE, SODIUM ASCORBATE and ASCORBIC ACID |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20080530 |
| Marketing Category Name | NDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
