Class II ยท Moderate risk
Folic Acid Tablets
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
National Drug Code
Is NDC 69315-0127-10 recalled?
Folic Acid · 1000 TABLET in 1 BOTTLE (69315-127-10)
Yes — this exact package was recalled
1 FDA recall names the code 69315-0127-10 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.
- Active ingredient
- Folic Acid
- Strength
- FOLIC ACID 1 mg/1
- Form
- Tablet · Oral
- Labeler
- Leading Pharma, LLC
- Type
- Human Prescription Drug
- Product code
- 69315-0127
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
- 69315-0308 ciprofloxacin 3
- 69315-0904 Lorazepam 2
- 69315-0118 Furosemide 1
- 69315-0167 Clomipramine Hydrochloride 1
- 69315-0905 Lorazepam 1
- 69315-0906 Lorazepam 1
Free recall alerts
Know the day your medication is recalled
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