NDC 43063-875

Promethazine Hydrochloride 12.5 mg tablet

On the label: PD-Rx Pharmaceuticals, Inc.. It's repackaged: PD-Rx Pharmaceuticals, Inc. rebottles it from KVK-TECH, Inc.'s NDC 10702-002.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Kvk-Tech, Inc.Newtown, PA, United StatesMakes it Serious problems, FDA actionMar 14, 2025 · 13 inspections, 3 with FDA action

Repackaging site

Product details

Generic drug
Promethazine: every company that makes it
Form
tablet, oral
Strength
12.5 mg
Approval
ANDA ANDA040712
On the market since
May 4, 2007
Package NDCs
43063-875-01
Official label
DailyMed (National Library of Medicine), updated May 22, 2026

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