NDC 70771-1540 – Meclizine Hydrochloride

Meclizine Hydrochloride 25 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC70771-1540

Product details

Brand name
Meclizine Hydrochloride
Generic name
Meclizine Hydrochloride
Labeler
Zydus Lifesciences Limited
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA213957
Marketed since
October 29, 2020
Listing expires
December 31, 2026
Pharmacologic class
Antiemetic

Active ingredients

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

Package NDC codes (5)

Package NDCDescriptionSince
70771-1540-01000 TABLET in 1 BOTTLE (70771-1540-0)Oct 29, 2020
70771-1540-1100 TABLET in 1 BOTTLE (70771-1540-1)Oct 29, 2020
70771-1540-330 TABLET in 1 BOTTLE (70771-1540-3)Oct 29, 2020
70771-1540-410 BLISTER PACK in 1 CARTON (70771-1540-4) / 10 TABLET in 1 BLISTER PACK (70771-1540-2)Oct 29, 2020
70771-1540-990 TABLET in 1 BOTTLE (70771-1540-9)Oct 29, 2020

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