NDC 55289-133
Hydralazine Hydrochloride 25 mg tablet, film coated
On the label: PD-Rx Pharmaceuticals, Inc.. It's repackaged from NDC 23155-002, made by Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. (Hydralazine Hydrochloride). That product's FDA listing has since ended, so its label and factories are no longer published.
Where the pills inside were made
This label doesn't name the factory that makes the drug (it lists 1 site that repackages it). 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 PD-Rx Pharmaceuticals, Inc. names for other drugs.
Product details
- Generic drug
- Hydralazine: every company that makes it
- Form
- tablet, film coated
- Strength
- 25 mg
- Approval
- ANDA ANDA086242
- On the market since
- Apr 6, 2007
- Package NDCs
55289-133-60- Official label
- DailyMed (National Library of Medicine), updated Mar 11, 2024
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