Class II · Moderate risk
Clindamycin HCl Capsule
CGMP Deviations - products manufactured in a shared facility with Ezetimibe tablets.
National Drug Code
Is NDC 70518-3772-00 recalled?
Clindamycin Hydrochloride · 30 CAPSULE in 1 BLISTER PACK (70518-3772-0)
Yes — this exact package was recalled
1 FDA recall names the code 70518-3772-00 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
- Clindamycin Hydrochloride
- Strength
- CLINDAMYCIN HYDROCHLORIDE 300 mg/1
- Form
- Capsule · Oral
- Labeler
- Remedyrepack INC.
- Type
- Human Prescription Drug
- Product code
- 70518-3772
Recalls naming this package
Class II · Moderate risk
Clindamycin HCl
CGMP Deviations
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
- 70518-1220 See recall 2
- 70518-1560 Doxazosin 2
- 70518-3519 See recall 2
- 70518-0060 See recall 1
- 70518-0064 See recall 1
- 70518-0218 Phenazopyridine Hydrochloride 1
Free recall alerts
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