LISINOPRIL AND HYDROCHLOROTHIAZIDE
- Product NDC
- 35356-778
- 11-digit product format
- 353560778
- Labeler code
- 35356
- Product ID
- 35356-778_4803bf3d-fb5c-4eac-ab42-e188711fa441
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LISINOPRIL AND HYDROCHLOROTHIAZIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA077912
- Marketing category
- ANDA
- Marketing start
- 2006-09-27
- Marketing end
- 0000-00-00
- Substance
- HYDROCHLOROTHIAZIDE; LISINOPRIL
- Active strength
- 25 mg/1; mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 35356-778-90 | 35356077890 | 90 TABLET in 1 BOTTLE (35356-778-90) | 90 tablet | 2006-09-27 | 0000-00-00 | No | No | Current |