NDC 68071-3529

Progesterone 200 mg capsule

On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Bionpharma Inc.'s NDC 69452-234.

United States: 1India: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Patheon Softgels Inc.High Point, NC, United StatesMakes it and tests it Problems found, fixed voluntarilyJul 17, 2025 · 10 inspections
Steril-Gene Life Sciences Private LimitedPuducherry, IndiaMakes it and tests it Serious problems, FDA actionAug 12, 2026 · 2 inspections, 1 with FDA action

Repackaging site

Product details

Generic drug
Progesterone: every company that makes it
Form
capsule, oral
Strength
200 mg
Approval
ANDA ANDA200900
On the market since
Nov 28, 2018
Package NDCs
68071-3529-3 68071-3529-6 68071-3529-8 68071-3529-9
Official label
DailyMed (National Library of Medicine), updated Nov 3, 2025

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