NDC 51079-075
Hydralazine Hydrochloride 25 mg tablet
On the label: Mylan Institutional Inc.. It's repackaged: Mylan Institutional Inc. rebottles it from Teva Pharmaceuticals USA, Inc.'s NDC 50111-327.
Where the pills inside were made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Teva Pharmaceuticals USA, Inc. names for other drugs.
Repackaging site
- Teva Pharmaceuticals USA, Inc., Fairfield, NJ, United States · makes it
Product details
- Generic drug
- Hydralazine: every company that makes it
- Form
- tablet, oral
- Strength
- 25 mg
- Approval
- ANDA ANDA088467
- On the market since
- Dec 26, 2007
- Package NDCs
51079-075-0151079-075-20- Official label
- DailyMed (National Library of Medicine), updated Jul 22, 2025
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