Lisinopril and Hydrochlorothiazide
- Product NDC
- 50090-7294
- 11-digit product format
- 500907294
- Labeler code
- 50090
- Product ID
- 50090-7294_5452862c-3a03-4d8e-9ece-5304d71a5a24
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lisinopril and Hydrochlorothiazide Tablets
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA076230
- Marketing category
- ANDA
- Marketing start
- 2015-03-12
- 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 |
|---|
| 50090-7294-0 | Lisinopril and Hydrochlorothiazide | 90 in 1 BOTTLE | TABLET | 90 | | 8 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-7294-0 | 50090729400 | 90 TABLET in 1 BOTTLE (50090-7294-0) | 90 tablet | 2024-10-09 | No | No | Historical |