NDC 50090-1069-01 - Carvedilol
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
- 50090-1069
- Requested NDC
- 50090-1069-01
- Package NDCs from labels
- 50090-1069-1, 50090-1069-3, 50090-1069-4, 50090-1069-0, 50090-1069-01
- Manufacturer
- A-S Medication Solutions
- Effective date
- 2025-08-13
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Carvedilol - A-S Medication Solutions | A-S Medication Solutions | 2025-08-13 | Human Prescription Drug Label |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 50090-1069-0 | Carvedilol | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | 28 | |
| 50090-1069-1 | Carvedilol | 180 in 1 BOTTLE | TABLET, FILM COATED | 180 | 28 | |
| 50090-1069-3 | Carvedilol | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | 28 | |
| 50090-1069-4 | Carvedilol | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | 28 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 50090-1069 | CARVEDILOL TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 26 | Current NDC, Legacy NDC, 4 package rows | 20250417_f5969d18-46c7-4f35-9668-2fd4f6bbeb17.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 50090-1069-0 | EA - Each | 50090-1069 | db7436a1-3a7e-40b2-872c-9f7b0c88e4b1 | 1 | 2021-08-05 |
| 50090-1069-1 | EA - Each | 50090-1069 | 40773752-74d6-4ead-8074-70a827889c01 | 1 | 2021-08-05 |
| 50090-1069-3 | EA - Each | 50090-1069 | 316f495a-89b8-408d-9e6d-f0e0b83be3f9 | 1 | 2022-12-07 |
| 50090-1069-4 | EA - Each | 50090-1069 | 409e4752-c858-44b9-9574-6f75c93fd002 | 1 | 2022-12-07 |
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 |
|---|---|---|---|---|---|---|
| Quality Choice Moisturizing Relief Eye Drops | DEXTRAN 70, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HCL | Chain Drug Marketing Association, Inc. | 1fb81759-5931-59c8-e063-6294a90a2277 | 2025-12-30 | Warnings | B697894SGQ |
| Quality Choice Lubricant Eye Drops Long Lasting | POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL | Chain Drug Marketing Assoc., Inc. | 0cd91c45-88a2-f88c-e063-6294a90ad127 | 2025-12-30 | Warnings | B697894SGQ |
| Archies Dry Eye Relief | POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL | Archie's Remedies | 07da099b-6b7f-984d-e063-6294a90a12ac | 2025-12-30 | Warnings | B697894SGQ |
| Equaline Multi-Symptom Eye Drops | POLYETHYLENE GLYCOL 400, TETRAHYDROZOLINE HCL, ZINC SULFATE | United Natural Foods, Inc. | fe467606-6d66-b695-e053-6294a90aab5d | 2025-12-30 | Warnings | B697894SGQ |
| SPF 30 Sunscreen | ZINC OXIDE, TITANIUM DIOXIDE | CLEURE | f5512f34-08ee-b0f6-e053-2a95a90ab5bd | 2025-12-29 | Warnings | 15FIX9V2JP |
| RE-NUTRIV ULTRA RADIANCE MAKEUP BROAD SPECTRUM SPF 20 | OCTINOXATE AND TITANIUM DIOXIDE | ESTEE LAUDER INC | 897b8edb-f089-4a49-baca-e05806b0a068 | 2025-12-29 | Warnings | 15FIX9V2JP |
| OI LIN SUNMILK SUNSCREEN SPF 30 | SUNSCREEN, TITANIUM DIOXIDE | Sunrider Manufacturing L.P. | 26b57314-1616-4ca4-b65f-a363c525b432 | 2025-12-29 | Warnings | 15FIX9V2JP |
| Carvedilol | CARVEDILOL | Northwind Health Company, LLC | a570b8ea-530d-4565-a091-bb9dbe4a6d8d | 2025-12-26 | Warnings, Adverse reactions | 200031 0K47UL67F2 |
| Carvedilol | CARVEDILOL | Northwind Health Company, LLC | df600dde-8ef9-52e3-e053-2a95a90a2dc0 | 2025-12-26 | Warnings, Adverse reactions | 200032 0K47UL67F2 |
| Carvedilol | CARVEDILOL | Northwind Health Company, LLC | f2a0407c-2e05-60eb-e053-2a95a90abc99 | 2025-12-26 | Warnings, Adverse reactions | 686924 0K47UL67F2 |
| StellaLife VEGA Oral Care | SPRAY | StellaLife, Inc. | b8ba495e-2cfe-092c-e053-2995a90a3fd3 | 2025-12-24 | Warnings | ETJ7Z6XBU4 |
| StellaLife VEGA Oral Care Recovery Kit | KIT | Homeocare Laboratories, Inc. | b701234a-0bd2-16d3-e053-2995a90a5b13 | 2025-12-24 | Warnings | ETJ7Z6XBU4 |
| TINTED FACIAL SUNSCREEN | ZINC OXIDE, TITANIUM DIOXIDE | Guangzhou Tata Biotechnology Co., Ltd. | 1259035e-9196-97de-e063-6394a90a9dec | 2025-12-22 | Warnings | 15FIX9V2JP |
| SPF 50 MINERAL SUNSCREEN LIP | ZINC OXIDE , TITANIUM DIOXIDE | Guangzhou Tata Biotechnology Co., Ltd. | 1c6f0964-9bee-1c06-e063-6294a90ac2a4 | 2025-12-22 | Warnings | 15FIX9V2JP |
| G.M. Collin FPS-SPF 50 UVA-UVB TINTED SUNSCREEN | ZINC OXIDE, TITANIUM DIOXIDE | LABORATOIRES DERMO-COSMETIK INC. | 468c90d7-3b9e-1641-e063-6394a90a928c | 2025-12-22 | Warnings | 15FIX9V2JP |
| TiZO3 | TITANIUM DIOXIDE, ZINC OXIDE | Fallien Cosmeceuticals Ltd. | 468d6476-127a-e9f0-e063-6294a90a3df9 | 2025-12-22 | Warnings | 15FIX9V2JP |
| YOUR SKIN BUT BETTER FAIR | TITANIUM DIOXIDE AND ZINC OXIDE | IT COSMETICS, LLC | 3e65ec1a-0ed9-433d-8da9-a6cb61829911 | 2025-12-22 | Warnings | 15FIX9V2JP |
| StellaLife VEGA Oral Care Peppermint Pain and Swelling Relief | ARNICA, CALENDULA, CHAMOMILLA, ECHINACEA ANGUSTIFOLIA, ECHINACEA PURPUREA, HEPAR SULPH CALC, HYPERICUM, LGNATIA, LEDUM PALUSTRE, RUTA, SILICEA, STAPHYSAGRIA | StellaLife, Inc. | 10d42c12-713a-f461-e063-6294a90a223b | 2025-12-22 | Warnings | ETJ7Z6XBU4 |
| StellaLife VEGA Oral Care Pain and Swelling Relief | ARNICA, CALENDULA, CHAMOMILLA, ECHINACEA ANGUSTIFOLIA, ECHINACEA PURPUREA, HEPAR SULPH CALC, HYPERICUM, LGNATIA, RUTA, STAPHYSAGRIA | StellaLife, Inc. | 10f8dee1-d5d3-0602-e063-6294a90a6dbf | 2025-12-22 | Warnings | ETJ7Z6XBU4 |
| THE MELT MIST Sheerest Mineral Mist Suncare for Body | TITANIUM DIOXIDE, ZINC OXIDE | Dune Suncare, Inc. | 465d3277-7798-512a-e063-6294a90a2065 | 2025-12-20 | Warnings | 15FIX9V2JP |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.