Lisinopril
- Product NDC
- 63739-350
- 11-digit product format
- 637390350
- Labeler code
- 63739
- Product ID
- 63739-350_b3b1cf6e-f150-24d2-e053-2a95a90a8130
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lisinopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- McKesson Corporation dba SKY Packaging
- Application
- ANDA076059
- Marketing category
- ANDA
- Marketing start
- 2002-07-01
- Marketing end
- 2021-02-28
- Substance
- LISINOPRIL
- Active strength
- 20 mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63739-350-10 | 63739035010 | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-350-10) > 10 TABLET in 1 BLISTER PACK | 10 blister pack | 2002-07-01 | 2021-02-28 | No | No | Current |
| 63739-350-43 | 63739035043 | 90 TABLET in 1 BOTTLE (63739-350-43) | 90 tablet | 2018-08-15 | 2021-02-28 | No | No | Current |