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Glutose
Glutose - 0574-0069-30 - (dextrose)
Drug Information of Glutose
| Product NDC: | 0574-0069 |
| Proprietary Name: | Glutose |
| Non Proprietary Name: | dextrose |
| Active Ingredient(s): | 15 g/37.5g & nbsp; dextrose |
| Administration Route(s): | ORAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Glutose
| Product NDC: | 0574-0069 |
| Labeler Name: | Paddock Laboratories, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED OTHER |
| Start Marketing Date: | 19960201 |
Package Information of Glutose
| Package NDC: | 0574-0069-30 |
| Package Description: | 3 TUBE in 1 CARTON (0574-0069-30) > 37.5 g in 1 TUBE |
NDC Information of Glutose
| NDC Code | 0574-0069-30 |
| Proprietary Name | Glutose |
| Package Description | 3 TUBE in 1 CARTON (0574-0069-30) > 37.5 g in 1 TUBE |
| Product NDC | 0574-0069 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | dextrose |
| Dosage Form Name | GEL |
| Route Name | ORAL |
| Start Marketing Date | 19960201 |
| Marketing Category Name | UNAPPROVED OTHER |
| Labeler Name | Paddock Laboratories, Inc. |
| Substance Name | DEXTROSE |
| Strength Number | 15 |
| Strength Unit | g/37.5g |
| Pharmaceutical Classes |
