Dextrose
- Product NDC
- 71872-7214
- 11-digit product format
- 718727214
- Labeler code
- 71872
- Product ID
- 71872-7214_faceeefa-0646-2e48-e053-6394a90a405f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dextrose monohydrate
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Medical Purchasing Solutions, LLC
- Application
- NDA019445
- Marketing category
- NDA
- Marketing start
- 2006-02-22
- Substance
- DEXTROSE MONOHYDRATE
- Active strength
- 250 mg/mL
- 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 |
|---|
| 71872-7214-1 | 71872721401 | 1 CARTON in 1 BAG (71872-7214-1) / 1 SYRINGE, PLASTIC in 1 CARTON / 10 mL in 1 SYRINGE, PLASTIC | 1 carton | 2020-06-05 | No | No | Historical |