NDC 72603-903-02
Labetalol Hydrochloride 200 mg/1
Labetalol Hydrochloride · TABLET
Labetalol Hydrochloride is a tablet containing labetalol hydrochloride at a strength of 200 mg/1. Manufactured by NorthStar Rx LLC.
Key Facts
- Brand Name
- Labetalol Hydrochloride
- Generic Name
- Labetalol Hydrochloride
- NDC Code (Package)
72603-903-02- NDC Code (Product)
72603-903- Manufacturer
- NorthStar Rx LLC
- Strength
- 200 mg/1
- Dosage Form
- TABLET
- Route
- ORAL
- Marketing Status
- Application #
- ANDA074787
- Marketing Start
- 03/19/2026
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.