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OsmoPrep
OsmoPrep - 54868-5889-0 - (SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE, SODIUM PHOSPHATE, DIBASIC ANHYDROUS)
Drug Information of OsmoPrep
| Product NDC: | 54868-5889 |
| Proprietary Name: | OsmoPrep |
| Non Proprietary Name: | SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE, SODIUM PHOSPHATE, DIBASIC ANHYDROUS |
| Active Ingredient(s): | .398; 1.102 g/1; g/1 & nbsp; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE, SODIUM PHOSPHATE, DIBASIC ANHYDROUS |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of OsmoPrep
| Product NDC: | 54868-5889 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021892 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20080530 |
Package Information of OsmoPrep
| Package NDC: | 54868-5889-0 |
| Package Description: | 32 TABLET in 1 BOTTLE, PLASTIC (54868-5889-0) |
NDC Information of OsmoPrep
| NDC Code | 54868-5889-0 |
| Proprietary Name | OsmoPrep |
| Package Description | 32 TABLET in 1 BOTTLE, PLASTIC (54868-5889-0) |
| Product NDC | 54868-5889 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE, SODIUM PHOSPHATE, DIBASIC ANHYDROUS |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20080530 |
| Marketing Category Name | NDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | SODIUM PHOSPHATE, DIBASIC ANHYDROUS; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE |
| Strength Number | .398; 1.102 |
| Strength Unit | g/1; g/1 |
| Pharmaceutical Classes |
