Dextrose
- Product NDC
- 0338-9143
- 11-digit product format
- 003389143
- Labeler code
- 0338
- Product ID
- 0338-9143_539f43d0-ac05-4261-a87d-8b34b07e0dd7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- dextrose monohydrate
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Baxter Healthcare Company
- Application
- NDA020179
- Marketing category
- NDA
- Marketing start
- 1992-12-07
- Substance
- DEXTROSE MONOHYDRATE
- Active strength
- 2.5 g/50mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| LX22YL083G | DEXTROSE MONOHYDRATE | 77938-63-7 | DEXTROSE MONOHYDRATE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 0338-9143-30 | 00338914330 | 30 BAG in 1 CARTON (0338-9143-30) / 50 mL in 1 BAG | 30 bag | 2021-02-19 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Dextrose | Baxter Healthcare Company | 2021-02-19 | HUMAN PRESCRIPTION DRUG LABEL | 14 |