Dextrose
- Product NDC
- 84549-517
- 11-digit product format
- 845490517
- Labeler code
- 84549
- Product ID
- 84549-517_3a38eb65-2341-a3ef-e063-6294a90ac75d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DEXTROSE MONOHYDRATE
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- ProPharma Distribution
- Application
- NDA019445
- Marketing category
- NDA
- Marketing start
- 2005-12-02
- Substance
- DEXTROSE MONOHYDRATE
- Active strength
- 25 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
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DEXTROSE MONOHYDRATE | 25 g/50mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | LX22YL083G |
| Rxcui | 727517 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 84549-517-16 | Dextrose | 50 mL in 1 SYRINGE, PLASTIC | INJECTION, SOLUTION | 50 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 84549-517-16 | 84549051716 | 50 mL in 1 SYRINGE, PLASTIC (84549-517-16) | 50 ml | 2025-08-27 | No | No | Historical |