NDC 58657-603-50
Labetalol Hydrochloride 200 mg/1
Labetalol Hydrochloride · TABLET, FILM COATED
Labetalol Hydrochloride is a tablet, film coated containing labetalol hydrochloride at a strength of 200 mg/1. Manufactured by Method Pharmaceuticals, LLC.
Key Facts
- Brand Name
- Labetalol Hydrochloride
- Generic Name
- Labetalol Hydrochloride
- NDC Code (Package)
58657-603-50- NDC Code (Product)
58657-603- Manufacturer
- Method Pharmaceuticals, LLC
- Strength
- 200 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- ANDA075215
- Drug Class
- beta-Adrenergic Blocker [EPC]
- Marketing Start
- 11/22/2019
Recall History
No Recall HistoryView Full Drug Page
Labetalol Hydrochloride — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.