NDC 70518-2191-01 - Amoxicillin
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
- 70518-2191
- Requested NDC
- 70518-2191-01
- Package NDCs from labels
- 70518-2191-0, 70518-2191-1, 70518-2191-2, 70518-2191-3, 70518-2191-4, 70518-2191-01
- Manufacturer
- REMEDYREPACK INC.
- Effective date
- 2026-07-21
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Amoxicillin - REMEDYREPACK INC. | REMEDYREPACK INC. | 2026-07-21 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70518-2191-0 | Amoxicillin | 20 in 1 BLISTER PACK | TABLET, FILM COATED | 20 | 16 | |
| 70518-2191-1 | Amoxicillin | 30 in 1 BLISTER PACK | TABLET, FILM COATED | 30 | 16 | |
| 70518-2191-2 | Amoxicillin | 20 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 20 | 16 | |
| 70518-2191-3 | Amoxicillin | 14 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 14 | 16 | |
| 70518-2191-4 | Amoxicillin | 14 in 1 BLISTER PACK | TABLET, FILM COATED | 14 | 16 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 70518-2191 | AMOXICILLIN TABLET, FILM COATED [REMEDYREPACK INC.] | 14 | Current NDC, Legacy NDC, 5 package rows | 20250309_9618d038-e880-47f6-b8d7-bbf8ab35364d.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 70518-2191-1 | EA - Each | 70518-2191 | 80304746-448c-448e-bec0-25b5d3865dac | 1 | 2026-01-08 |
| 70518-2191-2 | EA - Each | 70518-2191 | 3b38d850-848c-404b-a49a-fb9487dfb0d8 | 1 | 2026-01-08 |
| 70518-2191-3 | EA - Each | 70518-2191 | 11d546b2-3544-4211-8b6c-2965d628c23f | 1 | 2026-01-08 |
| 70518-2191-4 | EA - Each | 70518-2191 | 6be8b8d2-5362-4a08-9599-ee67df270b93 | 1 | 2026-01-08 |
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 |
|---|---|---|---|---|---|---|
| Amoxicillin and Clavulanate Potassium | AMOXICILLIN AND CLAVULANATE POTASSIUM | Asclemed USA, Inc. | f05a27dd-5ced-4f62-8a0c-548c3a033f5e | 2022-12-13 | Warnings, Adverse reactions | 804826J2HU |
| Defend Cold and Mucus | BRYONIA ALBA ROOT, EUPHRASIA STRICTA, CALCIUM SULFIDE, SODIUM CHLORIDE, PHOSPHORUS, ANEMONE PATENS, RUMEX CRISPUS ROOT, AND SILICON DIOXIDE | Hyland's Inc. | bb851be1-0528-4199-91e7-e09f994b2862 | 2022-12-12 | Warnings | ETJ7Z6XBU4 |
| basic care clearlax | POLYETHYLENE GLYCOL 3350 | Amazon.com Services LLC | 21897170-0d5e-4326-bebf-10258e0aca82 | 2022-12-08 | Warnings | G2M7P15E5P |
| 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 |
| POLYETHYLENE GLYCOL 3350 | POLYETHYLENE GLYCOL 3350 | Geri-Care Pharmaceutical Corp | f4c7eb80-d8d5-406d-90d0-9d17914d71f2 | 2022-11-24 | Warnings | G2M7P15E5P |
| 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 | 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 |
| Polyethylene Glycol 3350 | POLYETHYLENE GLYCOL 3350 | Gericare Pharmaceuticals | 5d0d2c14-24e6-45b4-92f6-4eaf5da72cdd | 2022-10-28 | Warnings | G2M7P15E5P |
| Equate ClearLAX | POLYETHYLENE GLYCOL 3350 | WALMART INC. | c5c13378-3c08-415f-8ab4-8a18d6300ca8 | 2022-09-08 | Warnings | G2M7P15E5P |
| 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 |
| injoy constipation relief | POLYETHYLENE GLYCOL 3350 | L. Perrigo Company | b2414517-04bf-4f29-951e-b867855078c3 | 2022-08-19 | Warnings | G2M7P15E5P |
| Amoxicillin | AMOXICILLIN | Proficient Rx LP | 7f75de78-2228-48e0-8405-bf631ca431ab | 2022-07-01 | Warnings, Adverse reactions | 804826J2HU |
| Good Sense Clear Lax | POLYETHYLENE GLYCOL 3350 | Proficient Rx LP | 0858a914-4812-4e4d-82f8-ecf93d43ef3b | 2022-07-01 | Warnings | G2M7P15E5P |
| Amoxicillin | AMOXICILLIN | Proficient Rx LP | de792ac6-4b3d-4d34-8e50-030b5bd830d7 | 2022-06-01 | Warnings, Adverse reactions | 804826J2HU |
| Amoxicillin and Clavulanate Potassium | AMOXICILLIN AND CLAVULANATE POTASSIUM | Proficient Rx LP | 3a7248ca-2855-433e-aabc-42f0bb0db118 | 2022-06-01 | Warnings, Adverse reactions | 804826J2HU |
| GAVILAX | POLYETHYLENE GLYCOL 3350 | Proficient Rx LP | 199d6173-3fad-49e4-88fe-bde7223ed4c3 | 2022-06-01 | Warnings | G2M7P15E5P |
| Amoxicillin | AMOXICILLIN | Proficient Rx LP | 756545f1-77af-49a0-a697-4cced31711d4 | 2022-06-01 | Warnings, Adverse reactions | 804826J2HU |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.