Dobutamine in Dextrose
- Product NDC
- 0409-0025
- 11-digit product format
- 004090025
- Labeler code
- 0409
- Product ID
- 0409-0025_1c7cc97c-e244-4a4b-a4a1-8b70ca812107
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dobutamine in Dextrose
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Hospira, Inc.
- Application
- NDA020201
- Marketing category
- NDA
- Marketing start
- 2026-03-16
- Substance
- DOBUTAMINE HYDROCHLORIDE
- Active strength
- 100 mg/100mL
- Pharmacologic classes
- Adrenergic beta-Agonists [MoA], beta-Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 0WR771DJXV | DOBUTAMINE HYDROCHLORIDE | 49745-95-1 | DOBUTAMINE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 0409-0025-10 | 00409002510 | 12 POUCH in 1 CASE (0409-0025-10) / 1 BAG in 1 POUCH / 250 mL in 1 BAG (0409-0025-01) | 12 pouch | 2026-03-16 | No | No | Historical |