Class II · Moderate risk
Potassium Citrate Extended-Release Tablets
Failed Tablet/Capsule Specifications: Tablet breakage
National Drug Code
Is NDC 42543-0407-01 recalled?
Potassium Citrate Extended Release · 100 TABLET in 1 BOTTLE (42543-407-01)
Yes — this exact package was recalled
1 FDA recall names the code 42543-0407-01 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
- Active ingredient
- Potassium Citrate
- Strength
- POTASSIUM CITRATE 10 meq/1
- Form
- Tablet · Oral
- Labeler
- Strides Pharma Inc.
- Type
- Human Prescription Drug
- Product code
- 42543-0407
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 42543-0052 See recall 1
- 42543-0408 Potassium Citrate Extended Release 1
Free recall alerts
Know the day your medication is recalled
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