Class II · Moderate risk
Tadalafil USP
CGMP Deviations:Noted during FDA inspection
National Drug Code
Is NDC 85702-0002-04 recalled?
Tadalafil · 500 g in 1 BAG (85702-002-04)
Yes — this exact package was recalled
1 FDA recall names the code 85702-0002-04 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
- Tadalafil
- Strength
- TADALAFIL 100 g/100g
- Form
- Powder
- Labeler
- Shoolin Pharma Chem LLP
- Type
- Bulk Ingredient
- Product code
- 85702-0002
Recalls naming this package
Class II · Moderate risk
Tadalafil USP
CGMP Deviations:Noted during FDA inspection
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
- 85702-0001 Sildenafil Citrate 3
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.