Lisinopril and Hydrochlorothiazide
- Product NDC
- 70518-0174
- 11-digit product format
- 705180174
- Labeler code
- 70518
- Product ID
- 70518-0174_47e3f082-89ce-b50f-e063-6294a90ad1a6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lisinopril and Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA077912
- Marketing category
- ANDA
- Marketing start
- 2017-01-23
- Substance
- HYDROCHLOROTHIAZIDE; LISINOPRIL
- Active strength
- 25; 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Lisinopril and Hydrochlorothiazide
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| HYDROCHLOROTHIAZIDE | 25 mg/1 |
| LISINOPRIL | 20 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 0J48LPH2TH, E7199S1YWR |
| Rxcui | 197887 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-0174-0 | Lisinopril and Hydrochlorothiazide | 30 in 1 BOTTLE, PLASTIC | TABLET | 30 | | 25 |
| 70518-0174-1 | Lisinopril and Hydrochlorothiazide | 90 in 1 BOTTLE, PLASTIC | TABLET | 90 | | 25 |
| 70518-0174-2 | Lisinopril and Hydrochlorothiazide | 100 in 1 BOTTLE, PLASTIC | TABLET | 100 | | 25 |
| 70518-0174-3 | Lisinopril and Hydrochlorothiazide | 30 in 1 BLISTER PACK | TABLET | 30 | | 25 |
| 70518-0174-4 | Lisinopril and Hydrochlorothiazide | 90 in 1 BOTTLE, PLASTIC | TABLET | 90 | | 25 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-0174 | LISINOPRIL AND HYDROCHLOROTHIAZIDE TABLET [REMEDYREPACK INC.] | 21 | Current NDC, Legacy NDC, 5 package rows | 20250424_408e797a-2cf3-4ee6-9f9b-179a8cf3d799.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 |
|---|
| 70518-0174-0 | 70518017400 | 30 TABLET in 1 BOTTLE, PLASTIC (70518-0174-0) | 30 tablet | 2017-01-23 | 0000-00-00 | No | No | Current |
| 70518-0174-1 | 70518017401 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-0174-1) | 90 tablet | 2017-02-02 | 0000-00-00 | No | No | Current |
| 70518-0174-2 | 70518017402 | 100 TABLET in 1 BOTTLE, PLASTIC (70518-0174-2) | 100 tablet | 2017-05-04 | | No | No | Current |
| 70518-0174-3 | 70518017403 | 30 TABLET in 1 BLISTER PACK (70518-0174-3) | 30 tablet | 2018-03-06 | 0000-00-00 | No | No | Current |
| 70518-0174-4 | 70518017404 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-0174-4) | 90 tablet | 2022-07-18 | 0000-00-00 | No | No | Current |