5% DEXTROSE
- Product NDC
- 51662-1413
- 11-digit product format
- 516621413
- Labeler code
- 51662
- Product ID
- 51662-1413_9f33d1ba-0e05-0cbd-e053-2a95a90af992
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- 5% DEXTROSE
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- HF Acquisition Co LLC, DBA HealthFirst
- Application
- NDA016367
- Marketing category
- NDA
- Marketing start
- 2019-10-14
- Marketing end
- 0000-00-00
- Substance
- DEXTROSE MONOHYDRATE
- Active strength
- 5 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
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 |
|---|
| 51662-1413-1 | 5% DEXTROSE | 50 mL in 1 BAG | INJECTION, SOLUTION | 50 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51662-1413 | 5% DEXTROSE INJECTION, SOLUTION [HF ACQUISITION CO LLC, DBA HEALTHFIRST] | 2 | Legacy NDC, 1 package rows | 20200223_94eb259b-1dd2-e32b-e053-2995a90a3f5b.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 |
|---|
| 51662-1413-1 | 51662141301 | 50 mL in 1 BAG (51662-1413-1) | 50 ml | 2019-10-14 | 0000-00-00 | No | No | Current |