LISINOPRIL AND HYDROCHLOROTHIAZIDE
- Product NDC
- 49999-924
- 11-digit product format
- 499990924
- Labeler code
- 49999
- Product ID
- 49999-924_3a4f6c35-b2a2-4ce6-9243-19c6212ae5a4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LISINOPRIL AND HYDROCHLOROTHIAZIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Quality Care Products LLC
- Application
- ANDA077912
- Marketing category
- ANDA
- Marketing start
- 2006-09-27
- Marketing end
- 0000-00-00
- Substance
- HYDROCHLOROTHIAZIDE; LISINOPRIL
- Active strength
- 13 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 |
|---|
| 49999-924-30 | 49999092430 | 30 TABLET in 1 BOTTLE (49999-924-30) | 30 tablet | 2006-09-27 | 0000-00-00 | No | No | Current |
| 49999-924-90 | 49999092490 | 90 TABLET in 1 BOTTLE (49999-924-90) | 90 tablet | 2006-09-27 | 0000-00-00 | No | No | Current |