NDC 0713-0135

Prochlorperazine 25 mg suppository

On the label: Cosette Pharmaceuticals, Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Cosette Pharmaceuticals NC Laboratories, LLCLincolnton, NC, United StatesMakes it, tests it, packages it and labels it Problems found, fixed voluntarilyJul 21, 2023 · 6 inspections

Product details

Generic drug
Prochlorperazine: every company that makes it
Form
suppository, rectal
Strength
25 mg
Approval
ANDA ANDA040058
On the market since
Nov 30, 1993
Package NDCs
0713-0135-10 0713-0135-12
Official label
DailyMed (National Library of Medicine), updated Dec 17, 2025

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