50% DEXTROSE
- Product NDC
- 51662-1216
- 11-digit product format
- 516621216
- Labeler code
- 51662
- Product ID
- 51662-1216_120092e4-46c1-f9e8-e063-6394a90ae574
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- 50% DEXTROSE
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- HF Acquisition Co LLC, DBA HealthFirst
- Application
- NDA019445
- Marketing category
- NDA
- Marketing start
- 2018-09-19
- 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
- 50% 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#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51662-1216-1 | 50% DEXTROSE | 1 in 1 CARTON | INJECTION, SOLUTION | 1 | | 5 |
| 51662-1216-1 | 50% DEXTROSE | 50 mL in 1 SYRINGE, PLASTIC | INJECTION, SOLUTION | 50 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51662-1216 | 50% DEXTROSE INJECTION, SOLUTION [HF ACQUISITION CO LLC, DBA HEALTHFIRST] | 5 | Current NDC, Legacy NDC, 2 package rows | 20240224_763b1cb8-1151-5f59-e053-2991aa0a4e01.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51662-1216-1 | 51662121601 | 1 SYRINGE, PLASTIC in 1 CARTON (51662-1216-1) / 50 mL in 1 SYRINGE, PLASTIC | 2018-09-19 | 0000-00-00 | No | No | Current |