DEXTROSE
- Product NDC
- 51662-1680
- 11-digit product format
- 516621680
- Labeler code
- 51662
- Product ID
- 51662-1680_4d2d3d3d-d96f-4005-e063-6394a90afd9a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DEXTROSE
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- HF Acquisition Co. LLC. DBA HealthFirst
- Application
- ANDA209448
- Marketing category
- ANDA
- Marketing start
- 2019-03-29
- Substance
- DEXTROSE MONOHYDRATE
- Active strength
- 100 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- 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 | 100 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | LX22YL083G |
| Rxcui | 1795480 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51662-1680-1 | DEXTROSE | 250 mL in 1 BAG | INJECTION, SOLUTION | 250 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 51662-1680-1 | 51662168001 | 250 mL in 1 BAG (51662-1680-1) | 250 ml | 2019-03-29 | No | No | Historical |