Class II ยท Moderate risk
My Way (Levonorgestrel)
Marketed Without an Approved NDA/ANDA: 2-pack configuration did not receive appropriate regulatory approval prior to release.
National Drug Code
Is NDC 43386-0622-31 recalled?
My Way
Yes — this exact package was recalled
1 FDA recall names the code 43386-0622-31 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
- Strength
- LEVONORGESTREL 1.5 mg/1
- Form
- Tablet · Oral
- Labeler
- Lupin Pharmaceuticals,Inc.
- Type
- Human OTC Drug
- Product code
- 43386-0622
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
- 43386-0069 Fluocinolone Acetonide 3
- 43386-0060 GaviLyte - C TM 2
- 43386-0450 Nitrofurantoin 2
- 43386-0541 Morphine Sulfate 2
- 43386-0038 Voriconazole 1
- 43386-0050 Gavilyte-N 1
Free recall alerts
Know the day your medication is recalled
Tell us what you take. When FDA posts a recall announcement or classifies a recall for one of your medications, we email you in plain English, with what to check. No account needed.