NDC 43063-086
Famotidine 20 mg tablet, film coated
On the label: PD-Rx Pharmaceuticals, Inc.. It's repackaged: PD-Rx Pharmaceuticals, Inc. rebottles it from Teva Pharmaceuticals USA, Inc.'s NDC 0172-5728.
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 Teva Pharmaceuticals USA, Inc. names for other drugs.
Repackaging site
- PD-Rx Pharmaceuticals Inc., Oklahoma City, OK, United States · repackages it
Recalls
- Jul 24, 2017 · Class II · Teva Pharmaceuticals USA
Failed Tablet/Capsule Specification; out of specification for tablet weight
Lots: Lot # 3429066, exp 06/2018
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Famotidine: every company that makes it
- Form
- tablet, film coated
- Strength
- 20 mg
- Approval
- ANDA ANDA075511
- On the market since
- Apr 16, 2001
- Package NDCs
43063-086-06- Official label
- DailyMed (National Library of Medicine), updated Oct 10, 2024
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