NDC 55111-252-79 - 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
- 55111-252
- Requested NDC
- 55111-252-79
- Package NDCs from labels
- 55111-252-30, 55111-252-01, 55111-252-05, 55111-252-10, 55111-252-79, 55111-252-78
- Manufacturer
- Dr. Reddy's Laboratories Limited | Dr. Reddys Laboratories Limited - FTO3
- Effective date
- 2018-12-05
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Carvedilol - Dr. Reddy's Laboratories Limited | Dr. Reddys Laboratories Limited - FTO3 | Dr. Reddy's Laboratories Limited | Dr. Reddys Laboratories Limited - FTO3 | 2018-12-05 | HUMAN PRESCRIPTION DRUG LABEL |
| Carvedilol - Preferred Pharmaceuticals, Inc | Preferred Pharmaceuticals, Inc | 2013-04-29 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 55111-252-01 | Carvedilol | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | 8 | |
| 55111-252-05 | Carvedilol | 500 in 1 BOTTLE | TABLET, FILM COATED | 500 | 8 | |
| 55111-252-10 | Carvedilol | 1000 in 1 BOTTLE | TABLET, FILM COATED | 1000 | 8 | |
| 55111-252-30 | Carvedilol | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | 8 | |
| 55111-252-78 | Carvedilol | 10 in 1 CARTON | TABLET, FILM COATED | 10 | 8 | |
| 55111-252-79 | Carvedilol | 10 in 1 BLISTER PACK | TABLET, FILM COATED | 10 | 8 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 55111-252-01 | EA - Each | 55111-252 | d2f137f5-0a50-4d3c-a2db-85df4473e458 | 1 | 2012-07-24 |
| 55111-252-05 | EA - Each | 55111-252 | 3e719c44-affa-47cd-b565-d89a313e8911 | 1 | 2012-07-24 |
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.
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| Mineffect acid indigestion and heartburn relief | ALUMINA, CALCAREA SILICATA, FERRUM METALLICUM, FERRUM PHOSPHORICUM, MAGNESIA MURIATICA, NATRUM NITRICUM, PHOSPHORUS, SILICEA, ZINCUM METALLICUM | Kadesh Incoporation Co,Ltd | 048367ff-a9bb-46a3-a835-aa3ab391eee4 | 2023-10-31 | Warnings | ETJ7Z6XBU4 |
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| LA MER THE RADIANT SKINTINT BROAD SPECTRUM SPF 30 | OCTINOXATE, OCTISALATE, AND TITANIUM DIOXIDE | MAX HUBER RESEARCH LAB INC | ecc942c7-5495-43b1-9ffa-d38be7891152 | 2023-10-30 | Warnings | 15FIX9V2JP |
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| SIMPLE TRUTH MINERAL BASED SPF 50 SUNSCREEN | TITANIUM DIOXIDE, ZINC OXIDE | THE KROGER COMPANY | a52872bf-cd0f-06da-e053-2995a90af28d | 2023-10-26 | Warnings | 15FIX9V2JP |
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| Diamond Luminous UV Defense Light Tinted Fluid Sunscreen Broad Spectrum SPF 40 | TITANIUM DIOXIDE, ZINC OXIDE | NATURA BISSE INTERNATIONAL SA | bf8b71c7-257b-0eb6-e053-2a95a90a3a4c | 2023-10-26 | Warnings | 15FIX9V2JP |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.