NDC 65862-040 – Lisinopril
Lisinopril 20 mg/1 · Tablet · Oral
Product NDC65862-040
Product details
- Brand name
- Lisinopril
- Generic name
- Lisinopril
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA077622
- Marketed since
- February 22, 2006
- Listing expires
- December 31, 2027
- Pharmacologic class
- Angiotensin Converting Enzyme Inhibitor
Active ingredients
- Lisinopril 20 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 65862-040-00 | 100 TABLET in 1 BOTTLE (65862-040-00) | Feb 22, 2006 |
| 65862-040-01 | 100 TABLET in 1 BOTTLE (65862-040-01) | Feb 22, 2006 |
| 65862-040-05 | 500 TABLET in 1 BOTTLE (65862-040-05) | Feb 22, 2006 |
| 65862-040-30 | 30 TABLET in 1 BOTTLE (65862-040-30) | Feb 22, 2006 |
| 65862-040-99 | 1000 TABLET in 1 BOTTLE (65862-040-99) | Feb 22, 2006 |
Recalls mentioning this NDC
- D-498-2013 Jun 5, 2013 · Class III
Labeling: Label Error on Declared Strength: Incorrect strength on side display panel of label
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