NDC 68071-3509

Phendimetrazine Tartrate 35 mg tablet

On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Elite Laboratories, Inc.'s NDC 64850-440.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Elite Laboratories, Inc.Northvale, NJ, United StatesMakes it Problems found, fixed voluntarilyAug 1, 2025 · 12 inspections, 1 with FDA action

Repackaging site

Product details

Generic drug
Phendimetrazine: every company that makes it
Form
tablet, oral
Strength
35 mg
Approval
ANDA ANDA040762
On the market since
Nov 20, 2012
Package NDCs
68071-3509-1 68071-3509-6 68071-3509-8 68071-3509-9
Official label
DailyMed (National Library of Medicine), updated Sep 27, 2024

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