NDC 61919-910
Prazosin Hydrochloride 1 mg capsule
On the label: Direct Rx. It's repackaged: Direct Rx 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
- Direct Rx, Dawsonville, GA, United States · repackages it
Recalls
- Oct 7, 2025 · Class II · Teva Pharmaceuticals USA, Inc
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.
Lots: a) NDC 0093-4067-01: Lot # 3010544A and 3010545A, Exp Date: 10/2025; Lot # 3010567A, Exp Date: 12/2025; Lot # 3010590A, Exp Date: 02/2026; Lot # 3010601A, 3010602A, 3010603A, Exp Date: 03/2026; Lot # 3010652A, 3010670A, 3010671A, Exp Date: 07/2026; Lot # 3010678A, 3010700A, 3010701A, Exp Date: 08/2…
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
- Strength
- 1 mg
- Approval
- ANDA ANDA071745
- On the market since
- Mar 12, 2018
- Package NDCs
61919-910-6061919-910-90- Official label
- DailyMed (National Library of Medicine), updated Oct 15, 2019
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?