Class II ยท Moderate risk
Posaconazole Delayed-Release Tablets
Failed Impurities/Degradation Specifications: High Out Of Specification degradation results.
National Drug Code
Is NDC 70377-0038-11 recalled?
Posaconazole · 60 TABLET, DELAYED RELEASE in 1 BOTTLE (70377-038-11)
Yes — this exact package was recalled
1 FDA recall names the code 70377-0038-11 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
- Posaconazole
- Strength
- POSACONAZOLE 100 mg/1
- Form
- Tablet, Delayed Release · Oral
- Labeler
- Biocon Phama Inc.
- Type
- Human Prescription Drug
- Product code
- 70377-0038
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
- 70377-0027 See recall 1
- 70377-0066 Prazosin hydrochloride 1
- 70377-0067 Prazosin hydrochloride 1
- 70377-0068 Prazosin hydrochloride 1
- 70377-0079 Atorvastatin Calcium 1
Free recall alerts
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