NDC 51672-4245-01 - 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
- 51672-4245
- Requested NDC
- 51672-4245-01
- Package NDCs from labels
- 51672-4245-1, 51672-4245-3, 51672-4245-01
- Manufacturer
- REMEDYREPACK INC.
- Effective date
- 2026-09-01
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Enalapril Maleate Tablets, USP | REMEDYREPACK INC. | 2026-09-01 | HUMAN PRESCRIPTION DRUG LABEL |
| Enalapril Maleate - Bryant Ranch Prepack | Bryant Ranch Prepack | 2026-08-24 | HUMAN PRESCRIPTION DRUG LABEL |
| Enalapril Maleate Tablets, USP | Golden State Medical Supply, Inc. | 2026-07-28 | 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 - A-S Medication Solutions | A-S Medication Solutions | 2023-10-02 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 51672-4245-1 | Enalapril Maleate | 100 in 1 BOTTLE | TABLET | 100 | 13 | |
| 51672-4245-3 | Enalapril Maleate | 1000 in 1 BOTTLE | TABLET | 1000 | 13 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 51672-4245 | ENALAPRIL MALEATE TABLET [TARO PHARMACEUTICALS U.S.A., INC.] | 13 | Current 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 |
|---|---|---|---|---|---|
| 51672-4245-1 | EA - Each | 51672-4245 | 4783b04f-762e-466c-b4ab-652d8e12ddeb | 1 | 2023-10-16 |
| 51672-4245-3 | EA - Each | 51672-4245 | ed82a21e-f396-472f-886f-b1bbea41b04d | 1 | 2023-10-16 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| Enalapril Maleate | ACTIVE INGREDIENT | 9O25354EPJ | ENALAPRIL MALEATE TABLET [TARO PHARMACEUTICALS U.S.A., INC.] | 6 | |
| Enalaprilat Anhydrous | ACTIVE MOIETY | Q508Q118JM | ENALAPRIL MALEATE TABLET [TARO PHARMACEUTICALS U.S.A., INC.] | 6 | |
| Ferric Oxide Red | INACTIVE INGREDIENT | 1K09F3G675 | ENALAPRIL MALEATE TABLET [TARO PHARMACEUTICALS U.S.A., INC.] | 6 | |
| Ferric Oxide Yellow | INACTIVE INGREDIENT | EX438O2MRT | ENALAPRIL MALEATE TABLET [TARO PHARMACEUTICALS U.S.A., INC.] | 6 | |
| Lactose Monohydrate | INACTIVE INGREDIENT | EWQ57Q8I5X | ENALAPRIL MALEATE TABLET [TARO PHARMACEUTICALS U.S.A., INC.] | 6 | |
| Magnesium Stearate | INACTIVE INGREDIENT | 70097M6I30 | ENALAPRIL MALEATE TABLET [TARO PHARMACEUTICALS U.S.A., INC.] | 6 | |
| Sodium Bicarbonate | INACTIVE INGREDIENT | 8MDF5V39QO | ENALAPRIL MALEATE TABLET [TARO PHARMACEUTICALS U.S.A., INC.] | 6 |
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 |
|---|---|---|---|---|---|---|
| Enalapril maleate | ENALAPRIL MALEATE | Northwind Health Company, LLC | f29ef93b-7380-2196-e053-2995a90a2ce3 | 2026-01-01 | Warnings, Adverse reactions | 858817 9O25354EPJ |
| Enalapril maleate | ENALAPRIL MALEATE | Northwind Health Company, LLC | f2a0bd73-0389-3f88-e053-2995a90a72e8 | 2026-01-01 | Warnings, Adverse reactions | 858810 9O25354EPJ |
| Enalapril maleate | ENALAPRIL MALEATE | Northwind Health Company, LLC | f2b3776b-02a1-311b-e053-2a95a90a2f9b | 2026-01-01 | Warnings, Adverse reactions | 858813 9O25354EPJ |
| Dermagesic | PRAMOXINE HCL, ZINC OXIDE, CALAMINE | Llorens Pharmaceutical International Division | bbff6b53-29da-45c1-8ccd-3e9df7f250e0 | 2025-12-31 | Warnings | 1K09F3G675 |
| Enalapril maleate | ENALAPRIL MALEATE | Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. | 5c49fb37-1f09-4965-b213-5580d3a30a11 | 2025-12-30 | Warnings, Adverse reactions | 858804 858810 858817 858813 9O25354EPJ |
| Medicated Cornstarch Baby Powder | ACTIVE CORN STARCH | Davion, Inc. | e39032d1-c8cd-4a41-af10-126970b8ad38 | 2025-12-29 | Warnings | O8232NY3SJ |
| Sodium Bicarbonate 10 gr | SODIUM BICARBONATE | GRAXCELL PHARMACEUTICAL, LLC | 897dbb09-fb47-4e03-8cae-bf76d48a7a03 | 2025-12-25 | Warnings | 8MDF5V39QO |
| Zegerid OTC | OMEPRAZOLE, SODIUM BICARBONATE | Riley Consumer Care LLC | 1d764fc5-8eae-4fc9-a2e9-3f1954a3ac05 | 2025-12-24 | Warnings | 8MDF5V39QO |
| BABY ANTI MONKEY BUTT DIAPER RASH | ZINC OXIDE, CALAMINE | Clarion Brands, LLC | e4424d74-f89c-5943-42e8-bf3a38e68619 | 2025-12-23 | Warnings | 1K09F3G675 |
| SODIUM BICARBONATE | SODIUM BICARBONATE | ProPharma Distribution | 3867f743-c2cf-a646-e063-6394a90a82e1 | 2025-12-18 | Warnings, Adverse reactions | 8MDF5V39QO |
| After Bite Advanced | SODIUM BICARBONATE | Tender Corporation d/b/a Adventure Ready Brands | 223d1de8-7940-bbdc-e063-6294a90a51d8 | 2025-12-18 | Warnings | 8MDF5V39QO |
| Enalapril maleate | ENALAPRIL MALEATE | Wilshire Pharmaceuticals, Inc. | c7934b45-eb6b-44c1-bd2c-ef0fa10850c1 | 2025-12-16 | Boxed warning, Warnings, Adverse reactions | 9O25354EPJ |
| Epaned | ENALAPRIL MALEATE | Azurity Pharmaceuticals, Inc. | e6dbda02-779e-420c-893d-d0fea09432be | 2025-12-16 | Boxed warning, Warnings, Adverse reactions | 9O25354EPJ |
| SinuCleanse | SODIUM BICARBONATE, SODIUM CHLORIDE | ASCENT CONSUMER PRODUCTS, INC. | beb842fa-2373-4f21-9631-ef20ee124584 | 2025-12-10 | Warnings | 8MDF5V39QO |
| All natural Saline Packets CareOne | SODIUM BICARBONATE, SODIUM CHLORIDE | FOODHOLD U.S.A. | e32f105d-65cd-8095-e053-2995a90a9b6b | 2025-12-10 | Warnings | 8MDF5V39QO |
| Alka-Seltzer Heartburn | ANHYDROUS CITRIC ACID, SODIUM BICARBONATE (HEAT-TREATED) | Bayer HealthCare LLC. | 55158e50-0327-2043-e054-00144ff8d46c | 2025-12-04 | Warnings | 8MDF5V39QO |
| Alka-Seltzer Extra Strength | ANHYDROUS CITRIC ACID, SODIUM BICARBONATE, AND ASPIRIN | Bayer HealthCare LLC. | 49b73bd5-6465-05eb-e054-00144ff88e88 | 2025-12-04 | Warnings | 8MDF5V39QO |
| Alka-Seltzer Gold | ALKA-SELTZER GOLD | Bayer HealthCare LLC. | 0824bedb-413b-2fa0-e054-00144ff88e88 | 2025-12-04 | Warnings | 8MDF5V39QO |
| Alka-Seltzer Original | ANHYDROUS CITRIC ACID, ASPIRIN, AND SODIUM BICARBONATE | Bayer HealthCare LLC. | 5be36a7f-7d1f-468d-9c29-92c8cd3ef1bc | 2025-12-04 | Warnings | 8MDF5V39QO |
| OMEPRAZOLE AND SODIUM BICARBONATE | OMEPRAZOLE AND SODIUM BICARBONATE | Aurohealth LLC | 88ad2e92-2228-49b2-bcee-1770fd30cb14 | 2025-12-04 | Warnings | 8MDF5V39QO |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.