NDC 60687-461-01
Labetalol Hydrochloride 300 mg/1
Labetalol Hydrochloride · TABLET, FILM COATED
Labetalol Hydrochloride is a tablet, film coated containing labetalol hydrochloride at a strength of 300 mg/1. Manufactured by American Health Packaging.
Key Facts
- Brand Name
- Labetalol Hydrochloride
- Generic Name
- Labetalol Hydrochloride
- NDC Code (Package)
60687-461-01- NDC Code (Product)
60687-461- Manufacturer
- American Health Packaging
- Strength
- 300 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- ANDA207743
- Marketing Start
- 07/16/2019
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.