Class II · Moderate risk
Chlorthalidone Tablets
Failed Dissolution Specifications
National Drug Code
Is NDC 64980-0599-10 recalled?
Chlorthalidone · 1000 TABLET in 1 BOTTLE (64980-599-10)
Yes — this exact package was recalled
1 FDA recall names the code 64980-0599-10 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
- Chlorthalidone
- Strength
- CHLORTHALIDONE 25 mg/1
- Form
- Tablet · Oral
- Labeler
- Rising Pharma Holdings, Inc.
- Type
- Human Prescription Drug
- Product code
- 64980-0599
Recalls naming this package
Class II · Moderate risk
Chlorthalidone Tablets
Failed Dissolution Specifications
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
- 64980-0514 Timolol Maleate 8
- 64980-0504 Cyproheptadine Hydrochloride 2
- 64980-0513 Timolol Maleate 2
- 64980-0104 Dibasic Sodium Phosphate, Monobasic Potassium Phosphate and Monobasic Sodium Phosphate 1
- 64980-0124 Diflorasone Diacetate 1
- 64980-0129 See recall 1
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