Dextrose
- Product NDC
- 0338-0172
- 11-digit product format
- 003380172
- Labeler code
- 0338
- Product ID
- 0338-0172_e30a7a3f-ea69-41c2-a58f-47a61601bad0
- 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
- 5 g/100mL
- 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
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DEXTROSE MONOHYDRATE | 5 g/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | LX22YL083G |
| Rxcui | 1795609, 1795616 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0338-0172-01 | Dextrose | 100 mL in 1 BAG | INJECTION | 100 | | 5 |
| 0338-0172-01 | Dextrose | 30 in 1 CARTON | INJECTION | 30 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0338-0172 | DEXTROSE (DEXTROSE MONOHYDRATE) INJECTION [BAXTER HEALTHCARE COMPANY] | 4 | Current NDC, Legacy NDC, 2 package rows | 20250426_9c80dfee-8923-4d1f-85b0-98bd68b94212.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0338-0172-01 | 00338017201 | 30 BAG in 1 CARTON (0338-0172-01) / 100 mL in 1 BAG | 30 bag | 2022-12-07 | 0000-00-00 | No | No | Current |