Dextrose
- Product NDC
- 0409-7936
- 11-digit product format
- 004097936
- Labeler code
- 0409
- Product ID
- 0409-7936_f22bcda2-771d-4ac9-b69b-f8fe36205568
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- dextrose
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Hospira, Inc.
- Application
- NDA018563
- Marketing category
- NDA
- Marketing start
- 2005-06-27
- Marketing end
- 2022-01-01
- Substance
- DEXTROSE MONOHYDRATE
- Active strength
- 50 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0409-7936-19 | 00409793619 | 12 POUCH in 1 CASE (0409-7936-19) > 1 BAG in 1 POUCH > 500 mL in 1 BAG | 12 pouch | 2005-06-27 | 2022-01-01 | No | No | Current |