Class II ยท Moderate risk
Phenoxybenzamine Hydrochloride Capsules
Failed Impurities/Degradation Specifications: Out of specification for unknown impurity.
National Drug Code
Is NDC 60219-1502-01 recalled?
Phenoxybenzamine hydrochloride · 100 CAPSULE in 1 BOTTLE (60219-1502-1)
Yes — this exact package was recalled
1 FDA recall names the code 60219-1502-01 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.
- Active ingredient
- Phenoxybenzamine hydrochloride
- Strength
- PHENOXYBENZAMINE HYDROCHLORIDE 10 mg/1
- Form
- Capsule · Oral
- Labeler
- Amneal Pharmaceuticals NY LLC
- Type
- Human Prescription Drug
- Product code
- 60219-1502
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
- 60219-2348 Tramadol Hydrochloride 1
Free recall alerts
Know the day your medication is recalled
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