NDC 68382-799 – Labetalol Hydrochloride

Labetalol Hydrochloride 200 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC68382-799

Product details

Brand name
Labetalol Hydrochloride
Generic name
Labetalol Hydrochloride
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA207743
Marketed since
December 5, 2017
Listing expires
December 31, 2027
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

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

Package NDC codes (4)

Package NDCDescriptionSince
68382-799-01100 TABLET, FILM COATED in 1 BOTTLE (68382-799-01)Dec 5, 2017
68382-799-05500 TABLET, FILM COATED in 1 BOTTLE (68382-799-05)Dec 5, 2017
68382-799-0630 TABLET, FILM COATED in 1 BOTTLE (68382-799-06)Dec 5, 2017
68382-799-1690 TABLET, FILM COATED in 1 BOTTLE (68382-799-16)Dec 5, 2017

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