Lisinopril
- Product NDC
- 53808-0703
- 11-digit product format
- 538080703
- Labeler code
- 53808
- Product ID
- 53808-0703_27c6283e-54e1-4ae0-a07a-dc71d92a6de2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LISINOPRIL
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- State of Florida DOH Central Pharmacy
- Application
- ANDA076059
- Marketing category
- ANDA
- Marketing start
- 2009-07-01
- Marketing end
- 0000-00-00
- Substance
- LISINOPRIL
- Active strength
- 20 mg/1
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| E7199S1YWR | LISINOPRIL | 83915-83-7 | LISINOPRIL |