NDC 43063-874

Promethazine Hydrochloride 25 mg tablet

On the label: PD-Rx Pharmaceuticals, Inc.. It's repackaged: PD-Rx Pharmaceuticals, Inc. rebottles it from KVK-TECH, Inc.'s NDC 10702-003.

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
25 mg
Approval
ANDA ANDA040712
On the market since
Jul 31, 2006
Package NDCs
43063-874-01 43063-874-02 43063-874-04 43063-874-05 43063-874-06 43063-874-10 43063-874-12 43063-874-15 43063-874-20 43063-874-25 43063-874-30 43063-874-79
Official label
DailyMed (National Library of Medicine), updated May 22, 2026

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