NDC 76420-282
Progesterone 200 mg capsule
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from Xiromed, LLC.'s NDC 70700-163.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Laboratorios Leon Farma SAU | Villaquilambre, Spain | Makes it | Problems found, fixed voluntarilyJul 11, 2025 · 8 inspections |
Repackaging site
- Asclemed USA Inc. dba Enovachem, Torrance, CA, United States · repackages it and relabels it
Product details
- Generic drug
- Progesterone: every company that makes it
- Form
- capsule, oral
- Strength
- 200 mg
- Approval
- ANDA ANDA205229
- On the market since
- Jan 8, 2021
- Package NDCs
76420-282-0176420-282-3076420-282-6076420-282-90- Official label
- DailyMed (National Library of Medicine), updated Sep 15, 2022
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