NDC 72603-903 – Labetalol Hydrochloride

Labetalol Hydrochloride 200 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC72603-903

Product details

Brand name
Labetalol Hydrochloride
Generic name
Labetalol Hydrochloride
Labeler
NorthStar Rx LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA074787
Marketed since
March 19, 2026
Listing expires
December 31, 2027
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

Uses, dosage, side effects and warnings for Labetalol Hydrochloride →

Package NDC codes (2)

Package NDCDescriptionSince
72603-903-01100 TABLET in 1 BOTTLE (72603-903-01)Mar 19, 2026
72603-903-02500 TABLET in 1 BOTTLE (72603-903-02)Mar 19, 2026

Other Labetalol Hydrochloride products