Labetalol Hydrochloride
- Product NDC
- 58657-906
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Labetalol Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Method Pharmaceuticals, LLC
- Application
- ANDA075215
- Marketing category
- ANDA
- Substance
- LABETALOL
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 58657-906-01 | 100 BLISTER PACK in 1 CARTON (58657-906-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (58657-906-10) | 2025-07-01 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Labetalol Hydrochloride | Method Pharmaceuticals, LLC | 2025-12-23 | HUMAN PRESCRIPTION DRUG LABEL | 11 |