NDC 57237-001-01 - Lansoprazole, Amoxicillin, Clarithromycin
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
- 57237-001
- Requested NDC
- 57237-001-01
- Package NDCs from labels
- 57237-001-01, 57237-001-14
- Manufacturer
- Rising Pharma Holdings, Inc. | Aurobindo Pharma Limited
- Effective date
- 2025-02-19
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Lansoprazole - Rising Pharma Holdings, Inc. | Aurobindo Pharma Limited | Rising Pharma Holdings, Inc. | Aurobindo Pharma Limited | 2025-02-19 | Human Prescription Drug Label |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 57237-001-14 | 2022-04-20 | C162847 | 48780-1 | 9d75b9d0-f016-f424-e053-dadaa90a57ce | Lansoprazole Delayed-Release Capsules USP, 30 mg, Amoxicillin Capsules USP, 500 mg, and Clarithromycin Tablets USP, 500 mg Rx only |
| 57237-001-14 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-f016-f424-e053-dadaa90a57ce | Lansoprazole Delayed-Release Capsules USP, 30 mg, Amoxicillin Capsules USP, 500 mg, and Clarithromycin Tablets USP, 500 mg Rx only |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 57237-001-01 | Lansoprazole, Amoxicillin, Clarithromycin | 1 in 1 BLISTER PACK | KIT | 1 | 13 | |
| 57237-001-14 | Lansoprazole, Amoxicillin, Clarithromycin | 14 in 1 CARTON | KIT | 14 | 13 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 57237-001-01 | EA - Each | 57237-001 | 01b6981f-89ce-49c1-917d-2a9c12aae7c1 | 1 | 2016-12-07 |
| 57237-001-14 | EA - Each | 57237-001 | fef45051-3218-445a-b742-a73b7e58fa0d | 1 | 2016-11-08 |
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 |
|---|---|---|---|---|---|---|
| Miranda Castros healing cell salts for bones, hair, nails and teeth Homeopathic Combination | CALCAREA FLUORICA, CALCAREA PHOSPHORICA, SILICEA | OHM PHARMA INC. | 044a7174-f7a3-490f-9cad-01f2665d7575 | 2022-12-02 | Warnings | ETJ7Z6XBU4 |
| Refresh Digital PF | CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN AND POLYSORBATE 80 | Allergan, Inc. | 97e83e68-6374-4df4-93f6-d707fc32748d | 2022-11-28 | Warnings | 6OZP39ZG8H |
| Refresh Digital | CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN, POLYSORBATE 80 | Allergan, Inc. | b2bd34d4-fab9-4f4b-9be2-5d30b55f5b81 | 2022-11-28 | Warnings | 6OZP39ZG8H |
| 4 Kids Cold and Mucus Nighttime | EUPHRASIA STRICTA,SILICON DIOXIDE, RUMEX CRISPUS ROOT, ANEMONE PULSATILLA, GOLDENSEAL, SODIUM CHLORIDE, PHOSPHORUS, ONION, BRYONIA ALBA ROOT, MATRICARIA CHAMOMILLA, ARABICA COFFEE BEAN, CALCIUM SULFIDE AND SULFUR | Hyland's Inc. | 6f7b2585-2f0e-5938-e053-2a91aa0aa9d1 | 2022-11-21 | Warnings | ETJ7Z6XBU4 |
| 4 Kids Complete Cold and Mucus | BRYONIA ALBA ROOT, EUPHRASIA STRICTA, CALCIUM SULFIDE, SODIUM CHLORIDE, PHOSPHORUS, ANEMONE PULSATILLA, RUMEX CRISPUS ROOT, AND SILICON DIOXIDE | Hyland's Inc. | ef39fe3d-a42d-4baa-9199-91f664feb432 | 2022-11-21 | Warnings | ETJ7Z6XBU4 |
| Amoxicillin | AMOXICILLIN | Asclemed USA, Inc. | fe9e12de-9be9-4211-9a58-c7ecd9e838d5 | 2022-11-02 | Warnings, Adverse reactions | 308191 804826J2HU |
| Amoxicillin and Clavulanate Potassium | AMOXICILLIN AND CLAVULANATE POTASSIUM | Proficient Rx LP | a0d22635-0e11-448d-b151-6f6168c65723 | 2022-11-01 | Warnings, Adverse reactions | 804826J2HU |
| Amoxicillin | AMOXICILLIN | Proficient Rx LP | 9cac2bf2-fb48-4e83-b953-61c4d55f7e19 | 2022-11-01 | Warnings, Adverse reactions | 804826J2HU |
| Lansoprazole | LANSOPRAZOLE | Proficient Rx LP | 3e3e63df-e2ad-420b-acb9-28e65ea6fb07 | 2022-10-01 | Warnings, Adverse reactions | 311277 0K5C5T2QPG |
| REFRESH OPTIVE Advanced | CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN, POLYSORBATE 80 | Allergan, Inc. | ebd0839e-2e1d-4e0e-986c-19f1f5c76358 | 2022-09-15 | Warnings | 6OZP39ZG8H |
| REFRESH OPTIVE Advanced | CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN, AND POLYSORBATE 80 | Allergan, Inc. | aaa943e4-7c38-4c5a-b7c0-5a656d8cafc0 | 2022-09-01 | Warnings | 6OZP39ZG8H |
| DEFENSE Hand Sanitizer | ISOPROPYL ALCOHOL | Walla Walla Environmental, Inc. | af49488d-5aeb-e3d9-e053-2a95a90afb04 | 2022-08-31 | Warnings | ND2M416302 |
| DEFENSE Hand Sanitizer | ISOPROPYL ALCOHOL | Walla Walla Environmental, Inc. | af498f92-6029-46b9-e053-2995a90a1c6d | 2022-08-31 | Warnings | ND2M416302 |
| Hendel Periodontal and Tooth Pain Relief | SODIUM BORATE, TRIBASIC CALCIUM PHOSPHATE, MERCURIUS SOLUBILIS, AND SILICON DIOXIDE | MediNatura Inc | f34e9f77-69fd-4c7f-9eea-2d721a4d27fb | 2022-08-22 | Warnings | ETJ7Z6XBU4 |
| LANSOPRAZOLE | LANSOPRAZOLE | Zydus Pharmaceuticals USA Inc. | 9b3869ad-f2f7-4954-b75c-5c23b8951635 | 2022-08-22 | Warnings, Adverse reactions | 0K5C5T2QPG |
| Magnesia Carbonica | MAGNESIA CARBONICA | Hahnemann Laboratories, INC. | e4310548-b362-a2c6-e053-2a95a90ac607 | 2022-07-19 | 0E53J927NA | |
| Amoxicillin | AMOXICILLIN | Proficient Rx LP | 7f75de78-2228-48e0-8405-bf631ca431ab | 2022-07-01 | Warnings, Adverse reactions | 804826J2HU |
| REFRESH Optive Mega-3 | CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN AND POLYSORBATE 80 | Allergan, Inc. | c5f2b3f2-2071-45bd-a010-67f848bc0233 | 2022-06-30 | Warnings | 6OZP39ZG8H |
| Lansoprazole | LANSOPRAZOLE | BluePoint Laboratories | 924c5a35-4804-4e14-a2fc-2b84d186d257 | 2022-06-20 | Warnings, Adverse reactions | 311277 0K5C5T2QPG |
| Amoxicillin | AMOXICILLIN | Proficient Rx LP | de792ac6-4b3d-4d34-8e50-030b5bd830d7 | 2022-06-01 | Warnings, Adverse reactions | 804826J2HU |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.