Lisinopril and Hydrochlorothiazide
- Product NDC
- 65862-044
- 11-digit product format
- 658620044
- Labeler code
- 65862
- Product ID
- 65862-044_5e2383b2-8c0d-450f-b681-74bfb12942a7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lisinopril and Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aurobindo Pharma Limited
- Application
- ANDA077606
- Marketing category
- ANDA
- Marketing start
- 2006-03-14
- Substance
- HYDROCHLOROTHIAZIDE; LISINOPRIL
- Active strength
- 12.5; 20 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
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Lisinopril and Hydrochlorothiazide
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| HYDROCHLOROTHIAZIDE | 12.5 mg/1 |
| LISINOPRIL | 20 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | E7199S1YWR, 0J48LPH2TH |
| Rxcui | 197885, 197886, 197887 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 65862-044-00 | Lisinopril and Hydrochlorothiazide | 100 in 1 BOTTLE | TABLET | 100 | | 20 |
| 65862-044-01 | Lisinopril and Hydrochlorothiazide | 100 in 1 BOTTLE | TABLET | 100 | | 20 |
| 65862-044-05 | Lisinopril and Hydrochlorothiazide | 500 in 1 BOTTLE | TABLET | 500 | | 20 |
| 65862-044-30 | Lisinopril and Hydrochlorothiazide | 30 in 1 BOTTLE | TABLET | 30 | | 20 |
| 65862-044-99 | Lisinopril and Hydrochlorothiazide | 1000 in 1 BOTTLE | TABLET | 1000 | | 20 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 65862-044 | LISINOPRIL AND HYDROCHLOROTHIAZIDE TABLET [AUROBINDO PHARMA LIMITED] | 20 | Current NDC, Legacy NDC, 5 package rows | 20240420_d7214539-6c3d-466a-a474-6fde096fa182.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 65862-044-00 | 65862004400 | 100 TABLET in 1 BOTTLE (65862-044-00) | 100 tablet | 2006-03-14 | 0000-00-00 | No | No | Current |
| 65862-044-01 | 65862004401 | 100 TABLET in 1 BOTTLE (65862-044-01) | 100 tablet | 2006-03-14 | 0000-00-00 | No | No | Current |
| 65862-044-05 | 65862004405 | 500 TABLET in 1 BOTTLE (65862-044-05) | 500 tablet | 2006-03-14 | 0000-00-00 | No | No | Current |
| 65862-044-30 | 65862004430 | 30 TABLET in 1 BOTTLE (65862-044-30) | 30 tablet | 2006-03-14 | 0000-00-00 | No | No | Current |
| 65862-044-59 | 65862004459 | 5000 TABLET in 1 BAG (65862-044-59) | 5000 tablet | 14-MAR-06 | | | | Current |
| 65862-044-99 | 65862004499 | 1000 TABLET in 1 BOTTLE (65862-044-99) | 1000 tablet | 2006-03-14 | 0000-00-00 | No | No | Current |