DEXTROSE MONOHYDRATE
- Product NDC
- 51662-1493
- 11-digit product format
- 516621493
- Labeler code
- 51662
- Product ID
- 51662-1493_9f454a28-ebef-2ce0-e053-2995a90a298c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DEXTROSE MONOHYDRATE
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- HF Acquisition Co LLC, DBA HealthFirst
- Application
- NDA016367
- Marketing category
- NDA
- Marketing start
- 2020-01-11
- 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 |
|---|
| 51662-1493-1 | DEXTROSE MONOHYDRATE | 1 in 1 POUCH | INJECTION, SOLUTION | 1 | | 2 |
| 51662-1493-1 | DEXTROSE MONOHYDRATE | 250 mL in 1 BAG | INJECTION, SOLUTION | 250 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51662-1493 | DEXTROSE MONOHYDRATE INJECTION, SOLUTION [HF ACQUISITION CO LLC, DBA HEALTHFIRST] | 2 | Legacy NDC, 2 package rows | 20200224_9be55a08-e93b-4b86-e053-2a95a90a94b9.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 |
|---|
| 51662-1493-1 | 51662149301 | 1 BAG in 1 POUCH (51662-1493-1) > 250 mL in 1 BAG | 1 bag | 2020-01-11 | 0000-00-00 | No | No | Current |