NDC 60760-991 – Labetalol Hydrochloride

Labetalol Hydrochloride 100 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC60760-991

Product details

Brand name
Labetalol Hydrochloride
Generic name
Labetalol Hydrochloride
Labeler
St. Mary's Medical Park Pharmacy
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA209603
Marketed since
March 12, 2025
Listing expires
December 31, 2027
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
60760-991-9090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-991-90)Mar 12, 2025

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