Labetalol hydrochloride
- Product NDC
- 50436-4364
- 11-digit product format
- 504364364
- Labeler code
- 50436
- Product ID
- 50436-4364_53a68870-5146-42eb-9925-7e748bf7afa3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Labetalol hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA075133
- Marketing category
- ANDA
- Marketing start
- 1998-08-03
- Marketing end
- 0000-00-00
- Substance
- LABETALOL HYDROCHLORIDE
- Active strength
- 100 mg/1
- 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