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Glycophos
Glycophos - 63323-241-20 - (SODIUM GLYCOLATE)
Drug Information of Glycophos
| Product NDC: | 63323-241 |
| Proprietary Name: | Glycophos |
| Non Proprietary Name: | SODIUM GLYCOLATE |
| Active Ingredient(s): | 216 mg/mL & nbsp; SODIUM GLYCOLATE |
| Administration Route(s): | INTRAVENOUS; INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Glycophos
| Product NDC: | 63323-241 |
| Labeler Name: | Fresenius Kabi USA, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE |
| Start Marketing Date: | 20130513 |
Package Information of Glycophos
| Package NDC: | 63323-241-20 |
| Package Description: | 10 VIAL, PLASTIC in 1 CARTON (63323-241-20) > 20 mL in 1 VIAL, PLASTIC |
NDC Information of Glycophos
| NDC Code | 63323-241-20 |
| Proprietary Name | Glycophos |
| Package Description | 10 VIAL, PLASTIC in 1 CARTON (63323-241-20) > 20 mL in 1 VIAL, PLASTIC |
| Product NDC | 63323-241 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | SODIUM GLYCOLATE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS; INTRAVENOUS |
| Start Marketing Date | 20130513 |
| Marketing Category Name | UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE |
| Labeler Name | Fresenius Kabi USA, LLC |
| Substance Name | SODIUM GLYCEROPHOSPHATE ANHYDROUS |
| Strength Number | 216 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
