NDC 43063-876

Promethazine Hydrochloride 50 mg tablet

On the label: PD-Rx Pharmaceuticals, Inc.. It's repackaged: PD-Rx Pharmaceuticals, Inc. rebottles it from KVK-TECH, Inc.'s NDC 10702-004.

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
50 mg
Approval
ANDA ANDA040712
On the market since
Jul 31, 2006
Package NDCs
43063-876-01 43063-876-04
Official label
DailyMed (National Library of Medicine), updated May 22, 2026

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