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 |
|---|---|---|---|---|---|---|
| MENS SPF50 ALL IN ONE SUNSCREEN | MENS SPF50 ALL IN ONE SUNSCREEN | Lance (Guangzhou) Biological Technology Co., Ltd. | 57074480-77fd-cc06-e063-6294a90a28d4 | 2026-07-20 | Warnings | 15FIX9V2JP |
| Yves Saint Laurent All Hours Foundation Sunscreen Broad Spectrum SPF 30 Luminous Matte Foundation | OCTINOXATE AND TITANIUM DIOXIDE | L'Oreal USA Products Inc | 5711364c-f9b4-bfa6-e063-6294a90ace4a | 2026-07-20 | Warnings | 15FIX9V2JP |
| Amoxicillin | AMOXICILLIN | HAWAII REPACK, INC. | bf130964-8386-4ab7-8d3b-fb0174670afc | 2026-07-17 | Warnings, Adverse reactions | 804826J2HU |
| Amoxicillin | AMOXICILLIN | PD-Rx Pharmaceuticals, Inc. | 18a4f555-a537-4c40-9bb2-dc3bd782fa27 | 2026-07-17 | Warnings, Adverse reactions | 804826J2HU |
| Amoxicillin and Clavulanate Potassium | AMOXICILLIN AND CLAVULANATE POTASSIUM | Preferred Pharmaceuticals Inc. | 1127a41b-14a1-4fe8-ae37-67ea5d760301 | 2026-07-16 | Warnings, Adverse reactions | 804826J2HU |
| Prid | ICHTHAMMOL, CALCIUM SULFIDE, CALENDULA OFFICINALIS FLOWERING TOP, ARNICA MONTANA, ECHINACEA ANGUSTIFOLIA, SILICON DIOXIDE, SULFUR | Hyland's Inc. | 49689eeb-7790-07f1-e063-6294a90a2df2 | 2026-07-16 | Warnings | ETJ7Z6XBU4 |
| AMOXICILLIN AND CLAVULANATE POTASSIUM | AMOXICILLIN AND CLAVULANATE POTASSIUM | REMEDYREPACK INC. | 6e1c6209-660f-4043-b6a6-eac5f7665ef9 | 2026-07-15 | Warnings, Adverse reactions | 804826J2HU |
| Leg Cramps PM | OYSTER SHELL CALCIUM CARBONATE, CRUDE, CAUSTICUM, MATRICARIA RECUTITA, CINCHONA OFFICINALIS BARK, COPPER, LYCOPODIUM CLAVATUM SPORE, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, TOXICODENDRON PUBESCENS LEAF, SILICON DIOXIDE, AND SULFUR | Hyland's Inc. | b0574a7e-88fa-417e-b6d5-60ced59eba47 | 2026-07-15 | Warnings | ETJ7Z6XBU4 |
| Amoxicillin | AMOXICILLIN | Preferred Pharmaceuticals Inc. | ad804b34-169c-44bf-a469-f1149433d96b | 2026-07-15 | Warnings, Adverse reactions | 308194 804826J2HU |
| Amoxicillin and Clavulanate Potassium | AMOXICILLIN AND CLAVULANATE POTASSIUM | HAWAII REPACK, INC. | 7fb0f56e-c098-49e4-b075-2eb8936582aa | 2026-07-13 | Warnings, Adverse reactions | 804826J2HU |
| Jacksons Cell Salts SILICA 12X 12 | SILICEA | Zettl Health Inc. | 5647dafc-1fff-6a25-e063-6294a90a8b4f | 2026-07-10 | ETJ7Z6XBU4 | |
| Amoxicillin | AMOXICILLIN | PD-Rx Pharmaceuticals, Inc. | 96057ce7-9516-4239-9974-5e9691b44c9b | 2026-07-09 | Warnings, Adverse reactions | 804826J2HU |
| Amoxicillin | AMOXICILLIN | Northwind Health Company, LLC | 1d0d8bc4-137e-ef10-e063-6294a90acf62 | 2026-07-09 | Warnings, Adverse reactions | 804826J2HU |
| Amoxicillin | AMOXICILLIN | Northwind Health Company, LLC | 26e257d5-5b98-3795-e063-6394a90a05bc | 2026-07-09 | Warnings, Adverse reactions | 804826J2HU |
| Amoxicillin | AMOXICILLIN | Northwind Health Company, LLC | 4ecefd37-9847-1d93-e063-6394a90a19f0 | 2026-07-09 | Warnings, Adverse reactions | 804826J2HU |
| Bombee Honey Daily Glow Shield Sunscreen | HOMOSALATE, OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE | ABT ASIA Inc. | 56112dff-b091-7a56-e063-6294a90a77d3 | 2026-07-08 | Warnings | 15FIX9V2JP |
| Stay Ageless Tinted Mineral Sunscreen | BROAD SPECTRUM SPF30 | DERMIO DERMATOLOGY LLC | 562f5b0d-6a10-305d-e063-6394a90a5980 | 2026-07-08 | Warnings | 15FIX9V2JP |
| Stay Ageless Tinted Mineral Sunscreen | BROAD SPECTRUM SPF30 | Suzanne's Skin2soul LLC | 562fbaa6-f93a-5ec4-e063-6294a90a9634 | 2026-07-08 | Warnings | 15FIX9V2JP |
| AMOXICILLIN AND CLAVULANATE POTASSIUM | AMOXICILLIN AND CLAVULANATE POTASSIUM | USAntibiotics, LLC | 7d4dfd6f-bd1a-4acc-8506-07fca08f8a38 | 2026-07-07 | Warnings, Adverse reactions | 804826J2HU |
| Amoxicillin | AMOXICILLIN | USAntibiotics, LLC | 06e5c07d-d95c-4955-8d35-a4703ca2359e | 2026-07-07 | Warnings, Adverse reactions | 804826J2HU |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.