NDC 53808-0776
Ranitidine Hydrochloride 150 mg tablet, film coated
On the label: State of Florida DOH Central Pharmacy. It's repackaged from NDC 0781-1883, made by Sandoz Inc (Ranitidine 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. 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 State of Florida DOH Central Pharmacy names for other drugs.
Product details
- Generic drug
- Ranitidine: every company that makes it
- Form
- tablet, film coated
- Strength
- 150 mg
- Approval
- ANDA ANDA074467
- On the market since
- Jul 1, 2009
- Package NDCs
53808-0776-1- Official label
- DailyMed (National Library of Medicine), updated Apr 13, 2010
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