NDC 51672-4038-01 - Enalapril Maleate
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 51672-4038
- Requested NDC
- 51672-4038-01
- Package NDCs from labels
- 51672-4038-1, 51672-4038-3, 51672-4038-01
- Manufacturer
- Bryant Ranch Prepack
- Effective date
- 2026-08-20
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Enalapril Maleate - Bryant Ranch Prepack | Bryant Ranch Prepack | 2026-08-20 | HUMAN PRESCRIPTION DRUG LABEL |
| Enalapril Maleate Tablets, USP | Golden State Medical Supply, Inc. | 2026-08-05 | HUMAN PRESCRIPTION DRUG LABEL |
| Enalapril Maleate Tablets, USP | Sun Pharmaceutical Industries, Inc. | Taro Pharmaceuticals Industries Ltd. | 2026-07-14 | HUMAN PRESCRIPTION DRUG LABEL |
| Enalapril Maleate Tablets, USP | Preferred Pharmaceuticals Inc. | 2024-04-15 | HUMAN PRESCRIPTION DRUG LABEL |
| Enalapril Maleate Tablets, USP | REMEDYREPACK INC. | 2024-02-21 | HUMAN PRESCRIPTION DRUG LABEL |
| Enalapril Maleate - A-S Medication Solutions | A-S Medication Solutions | 2023-12-12 | HUMAN PRESCRIPTION DRUG LABEL |
| Enalapril Maleate - St. Mary's Medical Park Pharmacy | St. Mary's Medical Park Pharmacy | 2021-10-06 | HUMAN PRESCRIPTION DRUG LABEL |
| Enalapril Maleate - Denton Pharma, Inc. dba Northwind Pharmaceuticals | Denton Pharma, Inc. dba Northwind Pharmaceuticals | 2020-07-07 | HUMAN PRESCRIPTION DRUG LABEL |
| Enalapril Maleate - Denton Pharma, Inc. dba Northwind Pharmaceuticals | Denton Pharma, Inc. dba Northwind Pharmaceuticals | 2020-03-26 | HUMAN PRESCRIPTION DRUG LABEL |
| Enalapril Maleate Tablets, USP | REMEDYREPACK INC. | 2019-09-15 | HUMAN PRESCRIPTION DRUG LABEL |
| Enalapril Maleate - DOH CENTRAL PHARMACY | DOH CENTRAL PHARMACY | 2019-01-17 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 51672-4038-1 | Enalapril Maleate | 100 in 1 BOTTLE | TABLET | 100 | 13 | |
| 51672-4038-3 | Enalapril Maleate | 1000 in 1 BOTTLE | TABLET | 1000 | 13 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 51672-4038 | ENALAPRIL MALEATE TABLET [TARO PHARMACEUTICALS U.S.A., INC.] | 13 | Current NDC, Legacy NDC, 2 package rows | 20230728_f103b9f9-e081-419d-a2d8-b86acda834dd.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 51672-4038-1 | EA - Each | 51672-4038 | a4d72af7-6ecd-4df1-b833-43669eab8d5c | 1 | 2013-02-13 |
| 51672-4038-3 | EA - Each | 51672-4038 | 687d907e-5dba-4a27-b4b7-48dc5c9a16d9 | 1 | 2013-02-13 |
DailyMed Socrata Ingredients#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| SODIUM BICARBONATE | SODIUM BICARBONATE | Richmond Pharmaceuticals, Inc. | fa10d93d-b3ed-4675-a117-f573d9e72bca | 2017-10-30 | Warnings | 8MDF5V39QO |
| Sodium Bicarbonate | SODIUM BICARBONATE | Exela Pharma Sciences, LLC | e9698a4f-1a95-4f28-a945-e8009d1d6dd4 | 2017-09-27 | Warnings, Adverse reactions | 8MDF5V39QO |
| Enalapril maleate and hydrochlorothiazide | ENALAPRIL MALEATE AND HYDROCHLOROTHIAZIDE | Dr. Reddy's Laboratories Limited | ed4a55a6-cd6a-c74a-cb93-4b45641691a0 | 2010-10-04 | Boxed warning, Warnings, Adverse reactions | 9O25354EPJ |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.