Esmolol Hydrochloride
- Product NDC
- 52584-049
- 11-digit product format
- 525840049
- Labeler code
- 52584
- Product ID
- 52584-049_c8b137d6-df03-476f-b654-0f19a40195b4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Esmolol Hydrochloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- General Injectables and Vaccines, Inc.
- Application
- ANDA076474
- Marketing category
- ANDA
- Marketing start
- 2015-09-10
- 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
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record