Class II · Moderate risk
Lanthanum Carbonate chewable tablets
Failed stability specifications: Out of specification for hardness test
National Drug Code
Is NDC 76282-0478-90 recalled?
Lanthanum carbonate · 9 BOTTLE in 1 PACKAGE (76282-478-90) / 10 TABLET, CHEWABLE in 1 BOTTLE (76282-478-13)
Yes — this exact package was recalled
2 FDA recalls name the code 76282-0478-90 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.
2 of these recalls are still ongoing.
- Active ingredient
- Lanthanum Carbonate
- Strength
- LANTHANUM CARBONATE 1000 mg/1
- Form
- Tablet, Chewable · Oral
- Labeler
- Exelan Pharmaceuticals, Inc.
- Type
- Human Prescription Drug
- Product code
- 76282-0478
Recalls naming this package
Class II · Moderate risk
Lanthanum Carbonate Chewable Tablets
Failed Tablet/Capsule Specifications: Complaints received of crushed and broken tablets.
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
- 76282-0103 Diclofenac Sodium 1
- 76282-0405 Gabapentin 1
- 76282-0673 Ramipril 1
- 76282-0708 See recall 1
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