DEXTROSE
- Product NDC
- 51662-1215
- 11-digit product format
- 516621215
- Labeler code
- 51662
- Product ID
- 51662-1215_11c3db4a-10d2-24e8-e063-6294a90a4167
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DEXTROSE
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- HF Acquisition Co LLC, DBA HealthFirst
- Application
- NDA019445
- Marketing category
- NDA
- Marketing start
- 2018-09-13
- 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 | 1795514 |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51662-1215-1 | DEXTROSE | 50 mL in 1 VIAL, SINGLE-DOSE | INJECTION, SOLUTION | 50 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51662-1215 | DEXTROSE INJECTION, SOLUTION [HF ACQUISITION CO LLC, DBA HEALTHFIRST] | 7 | Current NDC, Legacy NDC, 1 package rows | 20240220_75c902e8-50e7-a337-e053-2991aa0a2093.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 |
|---|
| 51662-1215-1 | 51662121501 | 50 mL in 1 VIAL, SINGLE-DOSE (51662-1215-1) | 50 ml | 2018-09-13 | 0000-00-00 | No | No | Current |