Lisinopril
- Product NDC
- 68645-550
- 11-digit product format
- 686450550
- Labeler code
- 68645
- Product ID
- 68645-550_c9eebd5b-3622-d2f5-e053-2a95a90a87db
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lisinopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Legacy Pharmaceutical Packaging, LLC
- Application
- ANDA077321
- Marketing category
- ANDA
- Marketing start
- 2006-01-13
- Marketing end
- 0000-00-00
- Substance
- LISINOPRIL
- Active strength
- 3 mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68645-550 | LISINOPRIL TABLET [LEGACY PHARMACEUTICAL PACKAGING, LLC] | 20 | Legacy NDC | 20241013_a9a9b82f-d02d-4a70-9af0-9100dddc16c9.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68645-550-54 | 68645055054 | 30 TABLET in 1 BOTTLE (68645-550-54) | 30 tablet | 2006-01-13 | 0000-00-00 | No | No | Current |