NDC 69238-1124-01 - Nadolol
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
- 69238-1124
- Requested NDC
- 69238-1124-01
- Package NDCs from labels
- 69238-1124-3, 69238-1124-9, 69238-1124-1, 69238-1124-01
- Manufacturer
- Amneal Pharmaceuticals NY LLC | Amneal Pharmaceuticals Private Limited
- Effective date
- 2026-05-12
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Nadolol - Amneal Pharmaceuticals NY LLC | Amneal Pharmaceuticals Private Limited | Amneal Pharmaceuticals NY LLC | Amneal Pharmaceuticals Private Limited | 2026-05-12 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 69238-1124-1 | Nadolol | 1000 in 1 BOTTLE | TABLET | 1000 | 9 | |
| 69238-1124-3 | Nadolol | 30 in 1 BOTTLE | TABLET | 30 | 9 | |
| 69238-1124-9 | Nadolol | 90 in 1 BOTTLE | TABLET | 90 | 9 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 69238-1124 | NADOLOL TABLET [AMNEAL PHARMACEUTICALS NY LLC] | 9 | Current NDC, Legacy NDC, 3 package rows | 20241011_e2e24b14-0169-4028-828a-894ad3c2ba55.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 69238-1124-9 | EA - Each | 69238-1124 | 59a05c5a-b29f-452c-a125-b46f3811855c | 1 | 2017-11-06 |
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 |
|---|---|---|---|---|---|---|
| Walgreens Eye Drops Advanced Relief 15mL | DEXTRAN 70, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HCI | Walgreen Company | 949f5560-fba7-2da8-e053-2995a90a23c2 | 2023-12-20 | Warnings | FZ989GH94E |
| Signature Care Eye Drops Advanced Relief | DEXTRAN 70, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HCL | Better Living Brands LLC | 5d7228ce-f108-4cc2-9aec-8b4548c3a155 | 2023-12-20 | Warnings | FZ989GH94E |
| Kroger Eye Drops Advanced Relief | DEXTRAN 70, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HYDROCHLORIDE | Kroger Company | f7ad77fc-d890-25b9-e053-6394a90a2b12 | 2023-12-20 | Warnings | FZ989GH94E |
| Equaline Advanced Relief Eye Drops | DEXTRAN 70, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HYDROCHLORIDE | United Natural Foods, Inc. | f7602789-179a-edfc-e053-6294a90a0844 | 2023-12-20 | Warnings | FZ989GH94E |
| Topcare Health Artificial Tears | POLYVINYL ALCOHOL, POVIDONE | Topco Associates LLC | 9c614c0e-5862-682f-e053-2a95a90abc09 | 2023-12-20 | Warnings | FZ989GH94E |
| TopCare Health Advanced Moisturizing Plus Redness Relief | DEXTRAN 70, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HCL | Topco Associates LLC | 9c6193a6-d822-1b27-e053-2995a90ab3cf | 2023-12-20 | Warnings | FZ989GH94E |
| HEB Advanced Eye Drops | DEXTRAN 70, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HYDROCHLORIDE | HEB Grocery Company, LP | f76281d6-3aea-349b-e053-6394a90afca2 | 2023-12-20 | Warnings | FZ989GH94E |
| Good Neighbor Pharmacy Artifical Tears Lubricant Eye Drops | POLYVINYL ALCOHOL, POVIDONE | Proficient Rx LP | 73e12596-6dd5-4cd2-83ed-992e1211b4b8 | 2023-12-01 | Warnings | FZ989GH94E |
| NADOLOL | NADOLOL | VGYAAN Pharmaceuticals LLC | 85b4b931-51c4-4326-88ea-708dde8323d4 | 2023-09-22 | Boxed warning, Warnings, Adverse reactions | 198007 198006 198008 FEN504330V |
| NADOLOL | NADOLOL | Alembic Pharmaceuticals Limited | 0bd202e3-c673-4945-b828-1a5bc6a896ae | 2023-06-08 | Warnings, Adverse reactions | 198007 198006 198008 FEN504330V |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.