DEXTROSE
- Product NDC
- 0338-9649
- 11-digit product format
- 003389649
- Labeler code
- 0338
- Product ID
- 0338-9649_66eb82f8-6755-42aa-b20c-192a640e8068
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- dextrose monohydrate
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Baxter Healthcare Corporation
- Application
- NDA016673
- Marketing category
- NDA
- Marketing start
- 1971-03-04
- Substance
- DEXTROSE MONOHYDRATE
- Active strength
- 2.5 g/50mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- DEXTROSE
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DEXTROSE MONOHYDRATE | 2.5 g/50mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | LX22YL083G |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0338-9649-75 | DEXTROSE | 75 in 1 CARTON | INJECTION, SOLUTION | 75 | | 10 |
| 0338-9649-75 | DEXTROSE | 50 mL in 1 BAG | INJECTION, SOLUTION | 50 | | 10 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0338-9649 | DEXTROSE (DEXTROSE MONOHYDRATE) INJECTION, SOLUTION [BAXTER HEALTHCARE CORPORATION] | 10 | Current NDC, 2 package rows | 20250516_36e9478c-5df0-4b47-b97d-de3626d7cb29.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 0338-9649-75 | 00338964975 | 75 BAG in 1 CARTON (0338-9649-75) / 50 mL in 1 BAG | 75 bag | 2024-08-09 | No | No | Current |