NDC 0555-0483
Amiloride Hydrochloride and Hydrochlorothiazide 5 mg / 50 mg tablet
On the label: Teva 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 Teva Pharmaceuticals USA, Inc. names for other drugs.
Product details
- Generic drug
- Amiloride and Hydrochlorothiazide: every company that makes it
- Form
- tablet, oral
- Strength
- 5 mg / 50 mg
- Approval
- ANDA ANDA071111
- On the market since
- Dec 1, 1989
- Package NDCs
0555-0483-020555-0483-05- Official label
- DailyMed (National Library of Medicine), updated Dec 27, 2022
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