NDC 68180-979 – Lisinopril
Lisinopril 40 mg/1 · Tablet · Oral
Product NDC68180-979
Product details
- Brand name
- Lisinopril
- Generic name
- Lisinopril
- Labeler
- Lupin Pharmaceuticals, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA077321
- Marketed since
- June 1, 2021
- Listing expires
- December 31, 2026
- Pharmacologic class
- Angiotensin Converting Enzyme Inhibitor
Active ingredients
- Lisinopril 40 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 68180-979-01 | 100 TABLET in 1 BOTTLE (68180-979-01) | Jun 1, 2021 |
| 68180-979-03 | 1000 TABLET in 1 BOTTLE (68180-979-03) | Jun 1, 2021 |
| 68180-979-30 | 5000 TABLET in 1 POUCH (68180-979-30) | Jun 1, 2021 |
Recalls mentioning this NDC
- D-1536-2022 Sep 21, 2022 · Class II
Presence of Foreign Substance: Foreign material (metal piece) embedded in one tablet. - D-1290-2020 Jun 17, 2020 · Class II
Product Mix Up: Lisinopril 10 mg tablets were found in Lisinopril 5 mg 1000-count bottle. - D-1079-2020 Apr 8, 2020 · Class II
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. - D-1077-2018 Aug 22, 2018 · Class II
Presence of Foreign Substance: Product complaint was received of metal contaminant observed in one tablet. - D-1503-2016 Sep 28, 2016 · Class III
CGMP Deviations: finished products manufactured using active pharmaceutical ingredients whose intermediates failed specifications. - D-1502-2016 Sep 28, 2016 · Class III
CGMP Deviations: finished products manufactured using active pharmaceutical ingredients whose intermediates failed specifications.
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