NDC 61919-307
Lisinopril 20 mg tablet
On the label: Direct Rx. It's repackaged: Direct Rx rebottles it from Lupin Pharmaceuticals, Inc.'s NDC 68180-515.
Where the pills inside were made
This label doesn't name the factory that makes the drug (it lists 3 sites that packages it). 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 Lupin Pharmaceuticals, Inc. names for other drugs.
Repackaging site
- Direct Rx, Dawsonville, GA, United States · repackages it
Recalls
- Sep 13, 2022 · Class II · Lupin Pharmaceuticals Inc.
Presence of Foreign Substance: Foreign material (metal piece) embedded in one tablet.
Lots: Lot # Q201182, exp. date March 2024 - May 28, 2020 · Class II · Lupin Pharmaceuticals Inc.
Product Mix Up: Lisinopril 10 mg tablets were found in Lisinopril 5 mg 1000-count bottle.
Lots: Lot # Q900683, Exp. 10/31/2022 - Apr 1, 2020 · Class II · Lupin Pharmaceuticals Inc.
Presence of Foreign Tablet/ Capsule: Product complaint received indicating mix-up of one lisinopril 5mg tablet inside of a 30 mg, 100-count bottle of Lisinopril Tablets.
Lots: Lot #: Q900580, Exp 9/2021 - Aug 13, 2018 · Class II · Lupin Pharmaceuticals Inc.
Presence of Foreign Substance: Product complaint was received of metal contaminant observed in one tablet.
Lots: Lot #: H800414, Exp. 12/2019 - Apr 6, 2016 · Class III · Lupin Pharmaceuticals Inc.
CGMP Deviations: finished products manufactured using active pharmaceutical ingredients whose intermediates failed specifications.
Lots: Batch number: H303487, H303488, H303489, Exp 09/16 - Apr 6, 2016 · Class III · Lupin Pharmaceuticals Inc.
CGMP Deviations: finished products manufactured using active pharmaceutical ingredients whose intermediates failed specifications.
Lots: Batch number: H303449, Exp 09/16
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Lisinopril: every company that makes it
- Form
- tablet
- Strength
- 20 mg
- Approval
- ANDA ANDA077321
- On the market since
- Jan 1, 2014
- Package NDCs
61919-307-3061919-307-6061919-307-90- Official label
- DailyMed (National Library of Medicine), updated Sep 19, 2019
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?