Lisinopril
- Product NDC
- 21695-345
- 11-digit product format
- 216950345
- Labeler code
- 21695
- Product ID
- 21695-345_81210afd-6505-4d38-ab83-e276ee4ce144
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lisinopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Rebel Distributors Corp
- Application
- ANDA077321
- Marketing category
- ANDA
- Marketing start
- 2008-02-01
- Marketing end
- 0000-00-00
- Substance
- LISINOPRIL
- Active strength
- 3 mg/1
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 21695-345-30 | Lisinopril | 30 in 1 BOTTLE | TABLET | 30 | | 2 |
| 21695-345-90 | Lisinopril | 90 in 1 BOTTLE | TABLET | 90 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 21695-345 | LISINOPRIL TABLET [REBEL DISTRIBUTORS CORP] | 2 | Legacy NDC, 2 package rows | 20111208_9b73c97f-b898-471f-be8a-96324a3e3b86.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 21695-345-30 | 21695034530 | 30 in 1 BOTTLE | Historical |
| 21695-345-90 | 21695034590 | 90 in 1 BOTTLE | Historical |