Lisinopril and Hydrochlorothiazide
- Product NDC
- 10544-236
- 11-digit product format
- 105440236
- Labeler code
- 10544
- Product ID
- 10544-236_468e33d9-bd82-4193-9270-c819f20b6b0f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lisinopril and Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Blenheim Pharmacal, Inc.
- Application
- ANDA077912
- Marketing category
- ANDA
- Marketing start
- 2012-04-30
- Marketing end
- 0000-00-00
- Substance
- HYDROCHLOROTHIAZIDE; LISINOPRIL
- Active strength
- 13 mg/1; mg/1
- Pharmacologic classes
- Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS],Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 10544-236-30 | Lisinopril and Hydrochlorothiazide | 30 in 1 BOTTLE | TABLET | 30 | | 12 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10544-236 | LISINOPRIL AND HYDROCHLOROTHIAZIDE TABLET [BLENHEIM PHARMACAL, INC.] | 12 | Legacy NDC, 1 package rows | 20151228_1aa9b1ec-cafd-4bc4-b424-e5f3e11242a5.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 10544-236-30 | 10544023630 | 30 in 1 BOTTLE | Historical |