NDC 12634-445
Hydrochlorothiazide 25 mg tablet
On the label: Apotheca, Inc.. It's repackaged from NDC 0527-1413, made by Lannett Company, 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. 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 Apotheca, Inc. names for other drugs.
Product details
- Generic drug
- Hydrochlorothiazide: every company that makes it
- Form
- tablet
- Strength
- 25 mg
- Approval
- ANDA ANDA084325
- On the market since
- Dec 21, 1996
- Package NDCs
12634-445-5012634-445-6012634-445-7112634-445-7812634-445-7912634-445-8512634-445-9012634-445-91- Official label
- DailyMed (National Library of Medicine), updated May 4, 2010
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?