NDC 64725-0045
Hydrochlorothiazide 12.5 mg capsule
On the label: TYA Pharmaceuticals. It's repackaged from NDC 23155-045, made by Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. (Hydrochlorothiazide). 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 and relabels 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 TYA Pharmaceuticals names for other drugs.
Product details
- Generic drug
- Hydrochlorothiazide: every company that makes it
- Form
- capsule
- Strength
- 12.5 mg
- Approval
- ANDA ANDA079237
- On the market since
- Dec 10, 2010
- Package NDCs
64725-0045-1- Official label
- DailyMed (National Library of Medicine), updated May 6, 2014
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