NDC 21695-809
Bisoprolol Fumarate and Hydrochlorothiazide 10 mg / 6.25 mg tablet, coated
On the label: Rebel Distributors Corp... It's repackaged from NDC 0185-0707, made by Eon Labs, Inc. (Bisoprolol Fumarate and 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 Rebel Distributors Corp.. names for other drugs.
Product details
- Generic drug
- Bisoprolol and Hydrochlorothiazide: every company that makes it
- Form
- tablet, coated
- Strength
- 10 mg / 6.25 mg
- Approval
- ANDA ANDA075579
- On the market since
- Sep 25, 2000
- Package NDCs
21695-809-30- Official label
- DailyMed (National Library of Medicine), updated Dec 10, 2010
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