Labetalol Hydrochloride
- Product NDC
- 55154-0184
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Labetalol Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Cardinal Health 107, LLC
- Application
- ANDA209603
- Marketing category
- ANDA
- Substance
- LABETALOL HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 55154-0184-0 | 10 BLISTER PACK in 1 BAG (55154-0184-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK | 20250506 | | No | Historical |
Related DailyMed Labels
| Set ID | Title | Manufacturer | Effective date | Type | Version |
|---|
| d3ca153c-25b2-4506-91bd-bf9d6a4c01fe | LABETALOL HYDROCHLORIDE TABLETS USP Rx only | Cardinal Health 107, LLC | 2026-03-20 | HUMAN PRESCRIPTION DRUG LABEL | 3 |