Class II · Moderate risk
Prazosin Hydrochloride Capsules
cGMP deviation: detection of Nitrosamine Drug Substance-Related Impurities, N-nitroso-prazosin impurity C (NNP) above acceptable limits.
National Drug Code
Is NDC 70377-0066-11 recalled?
Prazosin hydrochloride · 100 CAPSULE in 1 BOTTLE (70377-066-11)
Yes — this exact package was recalled
1 FDA recall names the code 70377-0066-11 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.
1 of these recalls is still ongoing.
- Active ingredient
- Prazosin hydrochloride
- Strength
- PRAZOSIN HYDROCHLORIDE 1 mg/1
- Form
- Capsule · Oral
- Labeler
- Biocon Pharma Inc.
- Type
- Human Prescription Drug
- Product code
- 70377-0066
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
- 70377-0038 Posaconazole 1
- 70377-0067 Prazosin hydrochloride 1
- 70377-0068 Prazosin hydrochloride 1
- 70377-0079 Atorvastatin Calcium 1
Free recall alerts
Know the day your medication is recalled
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