Dextrose
- Product NDC
- 52584-648
- 11-digit product format
- 525840648
- Labeler code
- 52584
- Product ID
- 52584-648_f8b43fa2-8812-4988-adba-5f62c4be7613
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dextrose Monohydrate
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- General Injectables & Vaccines, Inc
- Application
- NDA019445
- Marketing category
- NDA
- Marketing start
- 2010-07-01
- Marketing end
- 2024-03-01
- Substance
- DEXTROSE MONOHYDRATE
- Active strength
- 25 g/50mL
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 52584-648-02 | 52584064802 | 1 VIAL, SINGLE-DOSE in 1 BAG (52584-648-02) > 50 mL in 1 VIAL, SINGLE-DOSE | 2010-07-01 | 0000-00-00 | No | No | Current |