Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
RxRecalls Get alerts

National Drug Code

Is NDC 0378-1101-01 recalled?

Prazosin Hydrochloride · 100 CAPSULE in 1 BOTTLE, PLASTIC (0378-1101-01)

Yes — this exact package was recalled

1 FDA recall names the code 0378-1101-01 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
prazosin hydrochloride
Strength
PRAZOSIN HYDROCHLORIDE 1 mg/1
Form
Capsule · Oral
Labeler
Mylan Pharmaceuticals Inc.
Type
Human Prescription Drug
Product code
0378-1101

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