NDC 70710-1988
Hydralazine Hydrochloride 20 mg per 1 mL injection
On the label: Zydus Pharmaceuticals (USA) Inc..
Where it's 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 Zydus Pharmaceuticals (USA) Inc. names for other drugs.
Product details
- Generic drug
- Hydralazine: every company that makes it
- Form
- injection, intramuscular; intravenous
- Strength
- 20 mg per 1 mL
- Approval
- ANDA ANDA202938
- On the market since
- Apr 28, 2025
- Package NDCs
70710-1988-170710-1988-7- Official label
- DailyMed (National Library of Medicine), updated May 6, 2026
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