NDC 50090-1069-03 - 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
- 50090-1069-03
- Package NDCs from labels
- 50090-1069-1, 50090-1069-3, 50090-1069-4, 50090-1069-0, 50090-1069-03
- 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 |
|---|---|---|---|---|---|---|
| TOTAL DEFENSE REPAIR BROAD SPECTRUM SPF 34 Sunscreen (Tinted) | OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE AND ZINC OXIDE | Allergan, Inc. | 6a996e03-907f-4e6a-b232-0892b86956b0 | 2015-08-21 | Warnings | 15FIX9V2JP |
| Renewal Firming Day Broad Spectrum SPF 30 | TITANIUM DIOXIDE, ZINC OXIDE | BURT'S BEES, INC. | 18ceb5d8-4b76-6a54-e054-00144ff88e88 | 2015-06-18 | Warnings | 15FIX9V2JP |
| TiZO2 | TITANIUM DIOXIDE, ZINC OXIDE | Fallien Cosmeceuticals, LTD. | 30468afc-9616-4765-b046-12e97a0a7827 | 2010-12-20 | Warnings | 15FIX9V2JP |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.