NDC 68084-996

Prazosin Hydrochloride 1 mg capsule

On the label: American Health Packaging. It's repackaged: American Health Packaging rebottles it from Teva Pharmaceuticals USA, Inc.'s NDC 0093-4067.

Where the pills inside were made

This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Teva Pharmaceuticals USA, Inc. names for other drugs.

Repackaging site

Recalls

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug
Prazosin: every company that makes it
Form
capsule, oral
Strength
1 mg
Approval
ANDA ANDA071745
On the market since
Jul 12, 2018
Package NDCs
68084-996-01 68084-996-11
Official label
DailyMed (National Library of Medicine), updated Jan 8, 2025

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