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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Lumbar Drops 5013 | LUMBAR DROPS | Professional Complementary Health Formulas | ee6b54ea-fb6a-4723-8a0f-970aa82fea80 | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
| Rehydration Drops 2175 | REHYDRATION DROPS | Professional Complementary Health Formulas | 58cc2bd1-c530-43bf-876e-f30d4d95b8da | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
| Dysfunctional Bleeding Drops 2138 | DYSFUNCTIONAL BLEEDING DROPS | Professional Complementary Health Formulas | 3e674c1e-c64b-416d-962f-c03493e80085 | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
| Cervical Drops 5002 | CERVICAL DROPS | Professional Complementary Health Formulas | edd5f196-1423-4d4c-a8c1-89427c4f387e | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
| Asbestox 6005 | ASBESTOX | Professional Complementary Health Formulas | 90bc0d00-01e4-4134-809e-e216fd09852a | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
| Ledum Combination 9257 | LEDUM COMBINATION | Professional Complementary Health Formulas | 38b89b32-4915-487d-8b2d-250123487b15 | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
| Fourth Chakra (Heart) 7304 | FOURTH CHAKRA (HEART) | Professional Complementary Health Formulas | ef061447-42ae-43d0-b6f3-bf19a96ffe92 | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
| Spinal Drops 5025 | SPINAL DROPS | Professional Complementary Health Formulas | ca6d7250-9c9e-40a6-8d41-88aba33d21dd | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
| Anti-Scar Drops 2084 | ANTI-SCAR DROPS | Professional Complementary Health Formulas | ad0e9159-ed68-48aa-a7d1-7ff5c32ec304 | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
| Fifth Chakra (Throat) 7305 | FIFTH CHAKRA (THROAT) | Professional Complementary Health Formulas | b731f708-10a8-451f-8550-1e7302102b96 | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
| Sixth Chakra (Third Eye) 7306 | SIXTH CHAKRA (THIRD EYE) | Professional Complementary Health Formulas | 174024e7-e231-456c-bc00-48a358d7160a | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
| Injury Drops 2034 | INJURY DROPS | Professional Complementary Health Formulas | 024011a0-6471-4016-86d4-19eeb21f0d82 | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
| CARVEDILOL | CARVEDILOL | A-S Medication Solutions | 947baca7-f9c8-4821-b47b-53c45288613e | 2026-01-08 | Warnings, Adverse reactions | 200033 0K47UL67F2 |
| Third Chakra (Solar Plexus) 7303 | THIRD CHAKRA (SOLAR PLEXUS) | Professional Complementary Health Formulas | eea89c37-ab87-4cc7-8dfc-e7f42a580dd9 | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
| Hawaiian Blend Extreme Zinc SPF 30 | ZINC OXIDE, TITANIUM DIOXIDE | The Islander Group | 4084dd98-357f-4011-b0d4-db6536d2931f | 2026-01-07 | Warnings | 15FIX9V2JP |
| Hawaiian Blend Extreme Zinc SPF 50 | ZINC OXIDE, TITANIUM DIOXIDE | The Islander Group | 9b4acc5e-fdaf-4fcb-83a9-69e430dd43de | 2026-01-07 | Warnings | 15FIX9V2JP |
| Hawaiian Blend Sensitive Zinc SPF 50 | ZINC OXIDE, TITANIUM DIOXIDE | The Islander Group | b42261c5-fa6e-4bb3-93c0-97032ab9f716 | 2026-01-07 | Warnings | 15FIX9V2JP |
| BETA-GLUCAN MILD SUNSCREEN | TITANIUM DIOXIDE, ZINC OXIDE | IUNIK Co., Ltd | 47d6ad8b-1081-ee21-e063-6294a90a0e63 | 2026-01-07 | Warnings | 15FIX9V2JP |
| Solar Swipe Mineral Sunscreen SPF50 | SOLAR SWIPE MINERAL SUNSCREEN SPF50 | Guangzhou Fantesy Biotechnology Co.,Ltd | 47d75d61-5295-3eab-e063-6394a90a01c1 | 2026-01-07 | Warnings | 15FIX9V2JP |
| Lymphastat | BAPTISIA TINCTORIA, ECHINACEA (ANGUSTIFOLIA), LOBELIA INFLATA, LOMATIUM DISSECTUM, HYDRASTIS CANADENSIS, LUNG (SUIS), PHYTOLACCA DECANDRA, SYMPHYTUM OFFICINALE, ACONITUM NAPELLUS, ARSENICUM ALBUM, BELLADONNA, BRYONIA (ALBA), CAUSTICUM, EUPATORIUM PERFOLIATUM, FERRUM PHOSPHORICUM, GELSEMIUM SEMPERVIRENS, HYPERICUM PERFORATUM, KALI CARBONICUM, LACHESIS MUTUS, NATRUM SULPHURICUM, PHOSPHORUS, PULSATILLA (PRATENSIS), RHUS TOX, SILICEA, SULPHUR, PYROGENIUM | Energique, Inc. | ff95b833-3760-4e34-9636-90b423fc0d7b | 2026-01-07 | Warnings | ETJ7Z6XBU4 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.