Class III ยท Low risk
Portia (levonorgestrel and ethinyl estradiol)
Failed Tablet/Capsule Specifications: This recall is being carried out due to an out of specification result for appearance.
National Drug Code
Is NDC 0555-9020-58 recalled?
Portia · 6 POUCH in 1 CARTON (0555-9020-58) / 1 BLISTER PACK in 1 POUCH (0555-9020-79) / 1 KIT in 1 BLISTER PACK
Yes — this exact package was recalled
1 FDA recall names the code 0555-9020-58 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
- Levonorgestrel and Ethinyl Estradiol
- Form
- Kit
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Type
- Human Prescription Drug
- Product code
- 0555-9020
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
- 0555-0972 Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate 4
- 0555-9123 Jolessa 3
- 0555-0324 Hydroxyzine Pamoate 2
- 0555-0777 Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate 2
- 0555-0808 See recall 2
- 0555-0899 Estradiol 2
Free recall alerts
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