Lisinopril and Hydrochlorothiazide
- Product NDC
- 68788-8155
- 11-digit product format
- 687888155
- Labeler code
- 68788
- Product ID
- 68788-8155_61bf7e99-adb8-4311-bc00-ed4e0ac2d05c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lisinopril and Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA076194
- Marketing category
- ANDA
- Marketing start
- 2022-03-17
- 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 |
|---|
| 68788-8155-1 | 68788815501 | 100 TABLET in 1 BOTTLE, PLASTIC (68788-8155-1) | 100 tablet | 2022-03-17 | 0000-00-00 | No | No | Current |
| 68788-8155-3 | 68788815503 | 30 TABLET in 1 BOTTLE, PLASTIC (68788-8155-3) | 30 tablet | 2022-03-17 | 0000-00-00 | No | No | Current |
| 68788-8155-6 | 68788815506 | 60 TABLET in 1 BOTTLE, PLASTIC (68788-8155-6) | 60 tablet | 2022-03-17 | 0000-00-00 | No | No | Current |
| 68788-8155-9 | 68788815509 | 90 TABLET in 1 BOTTLE, PLASTIC (68788-8155-9) | 90 tablet | 2022-03-17 | 0000-00-00 | No | No | Current |