Dextrose
- Product NDC
- 0409-7930
- 11-digit product format
- 004097930
- Labeler code
- 0409
- Product ID
- 0409-7930_c1d63653-481f-425a-a260-77c6b502fb3b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- dextrose monohydrate
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Hospira, Inc.
- Application
- NDA018080
- Marketing category
- NDA
- Marketing start
- 2005-01-31
- Marketing end
- 2021-08-01
- Substance
- DEXTROSE MONOHYDRATE
- Active strength
- 10 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0409-7930-03 | 00409793003 | 24 POUCH in 1 CASE (0409-7930-03) > 1 BAG in 1 POUCH > 500 mL in 1 BAG | 24 pouch | 2005-01-31 | 2021-08-01 | No | No | Current |
| 0409-7930-09 | 00409793009 | 12 POUCH in 1 CASE (0409-7930-09) > 1 BAG in 1 POUCH > 1000 mL in 1 BAG | 12 pouch | 2005-03-31 | 2021-07-01 | No | No | Current |