NDC 63304-754 - Amoxicillin and Clavulanate Potassium
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
- 63304-754
- Package NDCs from labels
- 63304-754-03, 63304-754-20, 63304-754-01, 63304-754-21
- Manufacturer
- Physicians Total Care, Inc.
- Effective date
- 2010-05-21
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Amoxicillin and Clavulanate Potassium - Physicians Total Care, Inc. | Physicians Total Care, Inc. | 2010-05-21 | HUMAN PRESCRIPTION DRUG LABEL |
| Amoxicillin and clavulanate potassium - Ranbaxy Pharmaceuticals Inc. | Ranbaxy Pharmaceuticals Inc. | 2008-05-01 | HUMAN PRESCRIPTION DRUG LABELING |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 63304-754-01 | Amoxicillin and clavulanate potassium | 100 in 1 BOTTLE | TABLET, CHEWABLE | 100 | 1 | |
| 63304-754-03 | Amoxicillin and clavulanate potassium | 10 in 1 BOTTLE | TABLET, CHEWABLE | 10 | 1 | |
| 63304-754-20 | Amoxicillin and clavulanate potassium | 20 in 1 BOTTLE | TABLET, CHEWABLE | 20 | 1 | |
| 63304-754-21 | Amoxicillin and clavulanate potassium | 20 in 1 BLISTER PACK | TABLET, CHEWABLE | 20 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 63304-754 | AMOXICILLIN AND CLAVULANATE POTASSIUM (AMOXICILLIN AND CLAVULANATE POTASSIUM) POWDER, FOR SUSPENSION AMOXICILLIN AND CLAVULANATE POTASSIUM (AMOXICILLIN AND CLAVULANATE POTASSIUM) TABLET, CHEWABLE [RANBAXY PHARMACEUTICALS INC.] | 1 | 4 package rows | 20080602_b897c800-24a2-4e76-8668-498c5515c3d0.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 63304-754-20 | EA - Each | 63304-754 | 13dc1559-c20a-4ec1-afe6-8fbcbdf2a0f7 | 1 | 2013-02-13 |
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 |
|---|---|---|---|---|---|---|
| N-18 | OYSTER SHELL CALCIUM CARBONATE, CRUDE, SEPIA OFFICINALIS JUICE, SILICON DIOXIDE, NITRIC ACID, AND SUS SCROFA PINEAL GLAND | DNA Labs, Inc. | 3565c5d5-dc68-4f3f-99ec-30f8952393e0 | 2025-01-09 | Warnings | ETJ7Z6XBU4 |
| N-24 | METABOLIN | DNA Labs, Inc. | 559fca2b-1093-4bdf-be70-c453f87002c3 | 2025-01-09 | Warnings | ETJ7Z6XBU4 |
| NO-WEAK-NAILS | GRAPHITE, THUJA OCCIDENTALIS LEAFY TWIG, AND SILICON DIOXIDE | Miers Laboratories | 9158cd3f-4c27-40e9-bc07-fd560375c3a1 | 2025-01-09 | Warnings | ETJ7Z6XBU4 |
| Amoxicillin | AMOXICILLIN | NuCare Pharmaceuticals,Inc. | 6d7143e3-6a82-3613-e053-2a91aa0a8f65 | 2025-01-08 | Warnings, Adverse reactions | 804826J2HU |
| Amoxicillin | AMOXICILLIN | A-S Medication Solutions | 5b2a2e62-6fd2-4ab1-b936-8702e68233fa | 2025-01-08 | Warnings, Adverse reactions | 804826J2HU |
| Amoxicillin and Clavulanate Potassium | AMOXICILLIN AND CLAVULANATE POTASSIUM | Sandoz Inc | 99b7f40a-06f9-4b97-8eee-8e61e5106aad | 2025-01-08 | Warnings, Adverse reactions | Q42OMW3AT8 804826J2HU |
| Ferrum Silicicum Urtica | FERRUM SILICICUM URTICA | Uriel Pharmacy Inc. | 09829ac4-c074-7315-e063-6394a90adf59 | 2025-01-07 | Warnings | ETJ7Z6XBU4 |
| Amoxicillin | AMOXICILLIN | Preferred Pharmaceuticals Inc. | c84082fc-ea07-4e73-99c5-8356b957a1c5 | 2025-01-03 | Warnings, Adverse reactions | 804826J2HU |
| Amoxicillin | AMOXICILLIN | Northwind Pharmaceuticals, LLC | 26114563-c719-46da-b976-3e4271533f28 | 2025-01-02 | Warnings, Adverse reactions | 804826J2HU |
| Amoxicillin and Clavulanate Potassium | AMOXICILLIN AND CLAVULANATE POTASSIUM | NuCare Pharmaceuticals,Inc. | 9ba5b2b2-3c27-a2a8-e053-2a95a90a97cd | 2025-01-02 | Warnings, Adverse reactions | Q42OMW3AT8 804826J2HU |
| Amoxicillin and Clavulanate Potassium | AMOXICILLIN AND CLAVULANATE POTASSIUM | NuCare Pharmaceuticals,Inc. | abbebdc1-4410-76af-e053-2a95a90acb9c | 2025-01-02 | Warnings, Adverse reactions | 617430 Q42OMW3AT8 804826J2HU |
| MIMIBO PREMIUM TOOTH | SILICON DIOXIDE, TOCOPHEROL ACETATE, TETRASODIUM PYROPHOSPHATE | CONE MEDICAL Co., Ltd. | c0ff5df4-0b37-0b1b-e053-2a95a90a862c | 2025-01-02 | Warnings | ETJ7Z6XBU4 |
| MIMIBO PREMIUM TOOTH | SILICON DIOXIDE, TOCOPHEROL ACETATE, TETRASODIUM PYROPHOSPHATE | CONE MEDICAL Co., Ltd. | c101881a-5a12-2e04-e053-2a95a90a3f57 | 2025-01-02 | Warnings | ETJ7Z6XBU4 |
| NativeRemedies Acid Free-Flux | CALC PHOS 9X, CARBO VEG 6C, MAG CARB 6C, NAT PHOS 9X, SILICEA 9X | Silver Star Brands | d5012b1f-861e-40b8-e053-2a95a90a4fe2 | 2025-01-01 | Warnings | ETJ7Z6XBU4 |
| Mucus Clear Allergy Relief | ALLIU CEPA, CALC PHOS, EUPHRASIA, IGNATIA, KALI MUR, NAT MUR, NUX VOM, PULSATILLA, SILICA | Silver Star Brands | f49bdcc1-1939-6dc2-e053-2995a90a0a3b | 2025-01-01 | Warnings | ETJ7Z6XBU4 |
| NativeRemedies Gout-Gone | ANTIMON CRUD, BENZOICUM AC, LEDUM, NUX VOM, QUERCUS, RHODODENDRON, SILICEA | Silver Star Brands | f66b42f0-8f5f-1aca-e053-2a95a90ae396 | 2025-01-01 | Warnings | ETJ7Z6XBU4 |
| NeuropathEase | AGARICUS MUSC, ARSENICUM ALB, HYPERICUM, PHOS, SILICEA | Silver Star Brands | 7809e54a-018d-9cf6-e053-2a91aa0aedfe | 2025-01-01 | Warnings | ETJ7Z6XBU4 |
| AllergiClear-M | ADRENALINUM, CALCAREA FLUORICA, CALCAREA PHOSPHORICA, EUPHRASIA OFFICINALIS, HISTAMINUM HYDROCHLORICUM, KALI MURIATICUM, NATRUM MURIATICUM, SILICEA | Silver Star Brands | 9d36096b-022f-5cfa-e053-2995a90a381f | 2025-01-01 | Warnings | ETJ7Z6XBU4 |
| Amoxicillin | AMOXICILLIN | Advanced Rx Pharmacy of Tennessee, LLC | f4c36acc-828d-323b-e053-2a95a90a4d1c | 2024-12-31 | Warnings, Adverse reactions | 804826J2HU |
| Amoxicillin | AMOXICILLIN | NuCare Pharmaceuticals,Inc. | 5f8b3c58-ed9f-84a2-e053-2a91aa0ac8cf | 2024-12-27 | Warnings, Adverse reactions | 804826J2HU |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.