NDC 71610-851 – Hydroxyzine hydrochloride

Hydroxyzine Dihydrochloride 25 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71610-851

Product details

Brand name
Hydroxyzine hydrochloride
Generic name
Hydroxyzine hydrochloride
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA204279
Marketed since
August 20, 2014
Listing expires
December 31, 2026
Pharmacologic class
Antihistamine

Active ingredients

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

Package NDC codes (5)

Package NDCDescriptionSince
71610-851-3030 TABLET in 1 BOTTLE (71610-851-30)Aug 22, 2024
71610-851-5360 TABLET in 1 BOTTLE (71610-851-53)Aug 22, 2024
71610-851-6090 TABLET in 1 BOTTLE (71610-851-60)Aug 22, 2024
71610-851-70120 TABLET in 1 BOTTLE (71610-851-70)Aug 22, 2024
71610-851-80180 TABLET in 1 BOTTLE (71610-851-80)Aug 22, 2024

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