Class II ยท Moderate risk
TRIPENICOL S Antifungal Solution
CGMP Deviations; the firm discontinued required stability testing for products on the market still within expiry
National Drug Code
Is NDC 73352-0550-01 recalled?
Tripenicol S · 37.5 mL in 1 BOTTLE, WITH APPLICATOR (73352-550-01)
Yes — this exact package was recalled
1 FDA recall names the code 73352-0550-01 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.
1 of these recalls is still ongoing.
- Active ingredient
- Undecylenic acid
- Strength
- UNDECYLENIC ACID .25 g/mL
- Form
- Solution · Topical
- Labeler
- Trifluent Pharma LLC
- Type
- Human OTC Drug
- Product code
- 73352-0550
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
- 73352-0520 Tridergel 1
Free recall alerts
Know the day your medication is recalled
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