NDC 68001-335 – Lisinopril
Lisinopril 20 mg/1 · Tablet · Oral
Product NDC68001-335
Product details
- Brand name
- Lisinopril
- Generic name
- Lisinopril
- Labeler
- BluePoint Laboratories
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA077321
- Marketed since
- August 1, 2017
- Listing expires
- December 31, 2026
- Pharmacologic class
- Angiotensin Converting Enzyme Inhibitor
Active ingredients
- Lisinopril 20 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 68001-335-00 | 100 TABLET in 1 BOTTLE (68001-335-00) | Aug 1, 2017 |
| 68001-335-08 | 1000 TABLET in 1 BOTTLE (68001-335-08) | Aug 1, 2017 |
Recalls mentioning this NDC
- D-1413-2020 Aug 5, 2020 · Class II
Presence of Foreign Tablets/Capsules: Lisinopril Tablets USP, 20mg found in a 1000 count bottle of Lisinopril Tablets USP, 10mg
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