NDC 55695-031
Isoniazid 50 mg per 5 mL solution
On the label: Department of State Health Services, Pharmacy Branch. It's repackaged: Department of State Health Services, Pharmacy Branch rebottles it from CMP Pharma, Inc.'s NDC 46287-009.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Yuki Gosei Kogyo Co., Ltd. | Iwaki, Japan | Makes the active ingredient | Problems found, fixed voluntarilyFeb 6, 2026 · 7 inspections, 2 with FDA action |
Product details
- Generic drug
- Isoniazid: every company that makes it
- Form
- solution
- Strength
- 50 mg per 5 mL
- Approval
- ANDA ANDA088235
- On the market since
- Nov 11, 1983
- Package NDCs
55695-031-00- Official label
- DailyMed (National Library of Medicine), updated Mar 11, 2016
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