Mannitol
- Product NDC
- 0409-7715
- 11-digit product format
- 004097715
- Labeler code
- 0409
- Product ID
- 0409-7715_35c2d78f-a95c-4619-aff2-82ea456f7759
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- MANNITOL
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Hospira, Inc.
- Application
- NDA019603
- Marketing category
- NDA
- Marketing start
- 2005-09-19
- Marketing end
- 2021-12-08
- Substance
- MANNITOL
- Active strength
- 20 g/100mL
- Pharmacologic classes
- Increased Diuresis [PE],Osmotic Activity [MoA],Osmotic Diuretic [EPC]
- 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 |
|---|
| 0409-7715-02 | 00409771502 | 24 POUCH in 1 CASE (0409-7715-02) > 1 BAG in 1 POUCH > 250 mL in 1 BAG (0409-7715-12) | 24 pouch | 2005-10-18 | 2021-12-08 | No | No | Current |
| 0409-7715-03 | 00409771503 | 12 POUCH in 1 CASE (0409-7715-03) > 1 BAG in 1 POUCH > 500 mL in 1 BAG (0409-7715-13) | 12 pouch | 2005-09-19 | 2021-07-01 | No | No | Current |