NDC 0904-7451 – Labetalol Hydrochloride

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

Human Prescription Drug

Product NDC0904-7451

Product details

Brand name
Labetalol Hydrochloride
Generic name
Labetalol Hydrochloride
Labeler
Major Pharmaceuticals
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA209603
Marketed since
October 8, 2024
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
0904-7451-61100 BLISTER PACK in 1 CARTON (0904-7451-61) / 1 TABLET, FILM COATED in 1 BLISTER PACKOct 8, 2024

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