NDC 76420-580
Progesterone 200 mg capsule
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from Bionpharma Inc.'s NDC 69452-234.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Patheon Softgels Inc. | High Point, NC, United States | Makes it and tests it | Problems found, fixed voluntarilyJul 17, 2025 · 10 inspections |
| Steril-Gene Life Sciences Private Limited | Puducherry, India | Makes it and tests it | Serious problems, FDA actionAug 12, 2026 · 2 inspections, 1 with FDA action |
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 ANDA200900
- On the market since
- Nov 28, 2018
- Package NDCs
76420-580-1076420-580-3076420-580-6076420-580-90- Official label
- DailyMed (National Library of Medicine), updated May 7, 2025
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