NDC 0143-9233
Benztropine Mesylate 1 mg per 1 mL injection
On the label: Hikma Pharmaceuticals USA Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Hikma Farmaceutica (portugal), S.a | Terrugem Sintra, Portugal | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyApr 21, 2023 · 9 inspections, 1 with FDA action |
Product details
- Generic drug
- Benztropine: every company that makes it
- Form
- injection, intramuscular; intravenous
- Strength
- 1 mg per 1 mL
- Approval
- ANDA ANDA209442
- On the market since
- Oct 14, 2021
- Package NDCs
0143-9233-010143-9233-05- Official label
- DailyMed (National Library of Medicine), updated Apr 11, 2024
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