esmolol hydrochloride
- Product NDC
- 25021-314
- 11-digit product format
- 250210314
- Labeler code
- 25021
- Product ID
- 25021-314_1abbdd34-cd64-4043-a828-e52348913685
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- esmolol hydrochloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Sagent Pharmaceuticals
- Application
- ANDA208538
- Marketing category
- ANDA
- Marketing start
- 2020-01-15
- Marketing end
- 0000-00-00
- Substance
- ESMOLOL HYDROCHLORIDE
- Active strength
- 10 mg/mL
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 25021-314-10 | 25021031410 | 10 VIAL in 1 CARTON (25021-314-10) > 10 mL in 1 VIAL | 10 vial | 2020-01-15 | 0000-00-00 | No | No | Current |