NDC 23155-724 – Labetalol Hydrochloride

Labetalol Hydrochloride 200 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC23155-724

Product details

Brand name
Labetalol Hydrochloride
Generic name
Labetalol Hydrochloride
Labeler
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA074787
Marketed since
February 22, 2020
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
23155-724-01100 TABLET in 1 BOTTLE (23155-724-01)Feb 22, 2020
23155-724-05500 TABLET in 1 BOTTLE (23155-724-05)Feb 22, 2020

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