Class II · Moderate risk
Prazosin Hydrochloride
CGMP Deviations-Test results for N-nitroso Prazosin impurity C that are above the Carcinogenic Potency Categorization Approach (CPCA) acceptable intake limit for the above specified lots.
National Drug Code
Is NDC 0093-4069-05 recalled?
Prazosin Hydrochloride · 500 CAPSULE in 1 BOTTLE (0093-4069-05)
Yes — this exact package was recalled
1 FDA recall names the code 0093-4069-05 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 5 mg/1
- Form
- Capsule · Oral
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Type
- Human Prescription Drug
- Product code
- 0093-4069
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
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