Class II · Moderate risk
Mibelas 24 Fe
Failed Impurities/Degradation Specifications: Out of specification result observed in related substance test.
National Drug Code
Is NDC 68180-0911-13 recalled?
Mibelas 24 Fe
Yes — this exact package was recalled
2 FDA recalls name the code 68180-0911-13 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
- Norethindrone Acetate, Ethinyl Estradiol and Ferrous Fumarate
- Form
- Kit
- Labeler
- Lupin Pharmaceuticals, Inc.
- Type
- Human Prescription Drug
- Product code
- 68180-0911
Recalls naming this package
Class I · High risk
Mibelas 24 Fe
Contraceptive Tablets Out of Sequence- First 4 pills of the packet are brown, instead of the last four pills and the expiry/lot was not printed on the 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
- 68180-0723 Cefdinir 7
- 68180-0405 Cefixime 4
- 68180-0519 Lisinopril and Hydrochlorothiazide 4
- 68180-0422 Moxifloxacin 3
- 68180-0435 See recall 3
- 68180-0633 See recall 3
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