NDC 61919-312
Hydralazine Hydrochloride 25 mg tablet, film coated
On the label: Direct Rx. 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 Direct Rx 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
- Aug 13, 2019
- Package NDCs
61919-312-90- Official label
- DailyMed (National Library of Medicine), updated Jun 4, 2021
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?