NDC 10135-713-01
Labetalol Hydrochloride 300 mg/1
Labetalol · TABLET, FILM COATED
Labetalol Hydrochloride is a tablet, film coated containing labetalol at a strength of 300 mg/1. Manufactured by Marlex Pharmaceuticals Inc.
Key Facts
- Brand Name
- Labetalol Hydrochloride
- Generic Name
- Labetalol
- NDC Code (Package)
10135-713-01- NDC Code (Product)
10135-713- Manufacturer
- Marlex Pharmaceuticals Inc
- Strength
- 300 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- ANDA075215
- Drug Class
- beta-Adrenergic Blocker [EPC]
- Marketing Start
- 10/01/2020
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.