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Dextrose Monohydrate
Dextrose Monohydrate - 0548-3301-00 - (Dextrose Monohydrate)
Drug Information of Dextrose Monohydrate
| Product NDC: | 0548-3301 |
| Proprietary Name: | Dextrose Monohydrate |
| Non Proprietary Name: | Dextrose Monohydrate |
| Active Ingredient(s): | 500 mg/mL & nbsp; Dextrose Monohydrate |
| Administration Route(s): | PARENTERAL |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dextrose Monohydrate
| Product NDC: | 0548-3301 |
| Labeler Name: | Amphastar Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20000601 |
Package Information of Dextrose Monohydrate
| Package NDC: | 0548-3301-00 |
| Package Description: | 10 SYRINGE in 1 PACKAGE (0548-3301-00) > 50 mL in 1 SYRINGE |
NDC Information of Dextrose Monohydrate
| NDC Code | 0548-3301-00 |
| Proprietary Name | Dextrose Monohydrate |
| Package Description | 10 SYRINGE in 1 PACKAGE (0548-3301-00) > 50 mL in 1 SYRINGE |
| Product NDC | 0548-3301 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Dextrose Monohydrate |
| Dosage Form Name | INJECTION |
| Route Name | PARENTERAL |
| Start Marketing Date | 20000601 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Amphastar Pharmaceuticals, Inc. |
| Substance Name | DEXTROSE MONOHYDRATE |
| Strength Number | 500 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
