Labetalol Hydrochloride
- Product NDC
- 50436-4365
- 11-digit product format
- 504364365
- Labeler code
- 50436
- Product ID
- 50436-4365_fda9d15a-984f-463e-bfaa-ab0a25047342
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Labetalol Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA074787
- Marketing category
- ANDA
- Marketing start
- 1998-08-03
- Marketing end
- 0000-00-00
- Substance
- LABETALOL HYDROCHLORIDE
- Active strength
- 200 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