Lisinopril with Hydrochlorothiazide
- Product NDC
- 71335-0284
- 11-digit product format
- 713350284
- Labeler code
- 71335
- Product ID
- 71335-0284_1b8932c5-e777-44a2-b6ab-833644a2f7dc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lisinopril and Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076265
- Marketing category
- ANDA
- Marketing start
- 2002-07-08
- 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
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 71335-0284-1 | 2020-10-12 | C162847 | 48780-1 | 9d75b9cf-ebb2-f424-e053-dadaa90a57ce | b87f0e19-e0c5-4bf5-9cf8-37f569b16bb8 |
| 71335-0284-2 | 2020-10-12 | C162847 | 48780-1 | 9d75b9cf-ebb2-f424-e053-dadaa90a57ce | b87f0e19-e0c5-4bf5-9cf8-37f569b16bb8 |
| 71335-0284-3 | 2020-10-12 | C162847 | 48780-1 | 9d75b9cf-ebb2-f424-e053-dadaa90a57ce | b87f0e19-e0c5-4bf5-9cf8-37f569b16bb8 |
| 71335-0284-4 | 2020-10-12 | C162847 | 48780-1 | 9d75b9cf-ebb2-f424-e053-dadaa90a57ce | b87f0e19-e0c5-4bf5-9cf8-37f569b16bb8 |
| 71335-0284-1 | 2020-01-31 | C162847 | 48780-1 | 9d75b9cf-ebb2-f424-e053-dadaa90a57ce | b87f0e19-e0c5-4bf5-9cf8-37f569b16bb8 |
| 71335-0284-2 | 2020-01-31 | C162847 | 48780-1 | 9d75b9cf-ebb2-f424-e053-dadaa90a57ce | b87f0e19-e0c5-4bf5-9cf8-37f569b16bb8 |
| 71335-0284-3 | 2020-01-31 | C162847 | 48780-1 | 9d75b9cf-ebb2-f424-e053-dadaa90a57ce | b87f0e19-e0c5-4bf5-9cf8-37f569b16bb8 |
| 71335-0284-4 | 2020-01-31 | C162847 | 48780-1 | 9d75b9cf-ebb2-f424-e053-dadaa90a57ce | b87f0e19-e0c5-4bf5-9cf8-37f569b16bb8 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 71335-0284-1 | EA - Each | 71335-0284 | caeff5dd-dc15-4ddf-bf6b-4adf21e25963 | 1 | 2018-03-08 |
| 71335-0284-2 | EA - Each | 71335-0284 | 224c14d1-e22a-46ec-9d12-8d59e00ca95a | 1 | 2018-03-08 |
| 71335-0284-3 | EA - Each | 71335-0284 | 89cb419a-55d0-4c92-9c0b-2fe4124587d7 | 1 | 2018-03-08 |
| 71335-0284-4 | EA - Each | 71335-0284 | 69b2ed4e-a697-4cd5-ac27-19ef8beb8364 | 1 | 2018-03-08 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 71335-0284-1 | 71335028401 | 30 TABLET in 1 BOTTLE (71335-0284-1) | 30 tablet | 2015-08-28 | 0000-00-00 | No | No | Current |
| 71335-0284-2 | 71335028402 | 90 TABLET in 1 BOTTLE (71335-0284-2) | 90 tablet | 2015-08-28 | 0000-00-00 | No | No | Current |
| 71335-0284-3 | 71335028403 | 100 TABLET in 1 BOTTLE (71335-0284-3) | 100 tablet | 2015-08-28 | 0000-00-00 | No | No | Current |
| 71335-0284-4 | 71335028404 | 60 TABLET in 1 BOTTLE (71335-0284-4) | 60 tablet | 2015-08-28 | 0000-00-00 | No | No | Current |