NDC 0046-0749
Premarin 25 mg per 5 mL injection, powder, lyophilized, for solution
On the label: Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Pfizer Canada ULC | Brandon, Canada | Makes the active ingredient and tests it | No problems foundAug 3, 2023 · 4 inspections |
| Pfizer Ireland Pharmaceuticals Unlimited Company | Newbridge, Ireland | Makes the active ingredient | Problems found, fixed voluntarilySep 23, 2022 · 8 inspections |
Product details
- Generic drug
- Estrogens, Conjugated: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intramuscular; intravenous
- Strength
- 25 mg per 5 mL
- Approval
- NDA NDA010402
- On the market since
- Dec 1, 1956
- Package NDCs
0046-0749-05- Official label
- DailyMed (National Library of Medicine), updated May 30, 2025
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