NDC 60760-990

Hydroxyzine Hydrochloride 25 mg tablet, film coated

On the label: St. Mary's Medical Park Pharmacy. It's repackaged: St. Mary's Medical Park Pharmacy rebottles it from Rising Pharma Holdings, Inc.'s NDC 16571-114.

India: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Graviti Pharmaceuticals Private LimitedSangareddy, IndiaMakes it and tests it Problems found, fixed voluntarilyJul 28, 2026 · 2 inspections

Repackaging site

Product details

Generic drug
Hydroxyzine: every company that makes it
Form
tablet, film coated, oral
Strength
25 mg
Approval
ANDA ANDA217652
On the market since
Mar 19, 2025
Package NDCs
60760-990-30
Official label
DailyMed (National Library of Medicine), updated Jul 23, 2026

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