Esmolol Hydrochloride
- Product NDC
- 55154-2888
- 11-digit product format
- 551542888
- Labeler code
- 55154
- Product ID
- 55154-2888_5465feaf-c781-4b25-9793-6bcd8355cd81
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Esmolol Hydrochloride
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Cardinal Health
- Application
- NDA019386
- Marketing category
- NDA
- Marketing start
- 1986-12-31
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record