NDC 63304-515 - 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
- 63304-515
- Package NDCs from labels
- 63304-515-30, 63304-515-01, 63304-515-04
- Manufacturer
- Physicians Total Care, Inc.
- Effective date
- 2012-10-19
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Amoxicillin - Physicians Total Care, Inc. | Physicians Total Care, Inc. | 2012-10-19 | HUMAN PRESCRIPTION DRUG LABEL |
| AMOXICILLIN - Ranbaxy Pharmaceutical Inc. | Ranbaxy Pharmaceutical Inc. | 2008-05-19 | HUMAN PRESCRIPTION DRUG LABELING |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 63304-515-01 | AMOXICILLIN | 100 in 1 BOTTLE | TABLET, CHEWABLE | 100 | 1 | |
| 63304-515-04 | AMOXICILLIN | 250 in 1 BOTTLE | TABLET, CHEWABLE | 250 | 1 | |
| 63304-515-30 | AMOXICILLIN | 30 in 1 BOTTLE | TABLET, CHEWABLE | 30 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 63304-515 | AMOXICILLIN (AMOXICILLIN) CAPSULE AMOXICILLIN (AMOXICILLIN) TABLET, FILM COATED AMOXICILLIN (AMOXICILLIN) TABLET, CHEWABLE AMOXICILLIN (AMOXICILLIN) SUSPENSION [RANBAXY PHARMACEUTICAL INC.] | 1 | 3 package rows | 20080602_649d285c-8fcb-48dd-aa5e-2f34128102f5.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 63304-515-01 | EA - Each | 63304-515 | 646fd49d-eaa0-4648-b478-a2dba7f29801 | 1 | 2015-10-02 |
| 63304-515-04 | EA - Each | 63304-515 | 2c533ba4-0be6-49c3-9704-987a06e56b83 | 1 | 2015-10-02 |
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 |
|---|---|---|---|---|---|---|
| Multi-Phenolic | MANNOSE, 5-HYDROXYTRYPTOPHAN, ACETALDEHYDE, ACETYLCHOLINE CHLORIDE, ASCORBICUM ACIDUM, ASPARTAME, BUTYLATED HYDROXYTOLUENE, CAFFEIC ACID, CANDIDA ALBICANS, CINNAMIC ACID, CONIFERYL ALCOHOL, COUMARINUM, DOPAMINE HYDROCHLORIDE, ESTRADIOL, GABA (GAMMA-AMINOBUTYRIC ACID), GALLICUM ACIDUM, HISTAMINUM HYDROCHLORICUM, HYDROCORTISONE, INDOLUM, L-DOPA, L-PHENYLALANINE, MELATONIN, MENADIONE, NOREPINEPHRINE (BITARTRATE), PETROSELINUM CRISPUM, PHENYL ISOTHIOCYANATE, PIPERINE, PROGESTERONE, PYRROLE, QUERCETIN, | Energique, Inc. | 492b412a-01cc-48f2-bcdc-6fffcc651963 | 2024-08-23 | Warnings | Z0H242BBR1 |
| Amoxicillin | AMOXICILLIN | Asclemed USA, Inc. | a18751fa-6202-4ae2-950a-a3f1dc9a8afd | 2024-08-21 | Warnings, Adverse reactions | 308192 308194 804826J2HU |
| Amoxicillin | AMOXICILLIN | Asclemed USA, Inc. | 9cd42f6f-cc7a-43f5-98dd-a5d6210933ae | 2024-08-14 | Warnings, Adverse reactions | 308182 308191 804826J2HU |
| Amoxicillin | AMOXICILLIN | NuCare Pharmaceuticals,Inc. | 5780c9e4-5e22-270c-e053-2a91aa0a36ba | 2024-08-14 | Warnings, Adverse reactions | 804826J2HU |
| Amoxicillin | AMOXICILLIN | Rising Pharma Holdings, Inc. | 554239db-69fe-405a-910a-d9f9e3f8b6ed | 2024-08-06 | Warnings, Adverse reactions | 313850 308189 804826J2HU |
| Amoxicillin and Clavulanate Potassium | AMOXICILLIN AND CLAVULANATE POTASSIUM | Proficient Rx LP | 474c822b-dc3d-4a55-8159-2b4b799d535b | 2024-08-01 | Warnings, Adverse reactions | 804826J2HU |
| Amoxicillin | AMOXICILLIN | Proficient Rx LP | c8e5ad7d-09b7-41d9-8cb0-467b3e8df74f | 2024-08-01 | Warnings, Adverse reactions | 804826J2HU |
| Amoxicillin and Clavulanate Potassium | AMOXICILLIN AND CLAVULANATE POTASSIUM | NuCare Pharmaceuticals,Inc. | 5d074fe6-1ee0-40d8-e053-2a91aa0a7549 | 2024-07-15 | Warnings, Adverse reactions | 804826J2HU |
| Amoxicillin | AMOXICILLIN | NuCare Pharmaceuticals,Inc. | 8f8b1fe6-23cb-2105-e053-2a95a90aeede | 2024-07-10 | Warnings, Adverse reactions | 308182 804826J2HU |
| Amoxicillin and Clavulanate Potassium | AMOXICILLIN AND CLAVULANATE POTASSIUM | NorthStar Rx LLC | f0a6d21d-203f-4fde-b010-a2730b86b491 | 2024-07-09 | Warnings, Adverse reactions | 804826J2HU |
| Amoxicillin | AMOXICILLIN | Rising Pharma Holdings, Inc. | bb7733f8-6aad-4273-84a0-ef472630203f | 2024-07-07 | Warnings, Adverse reactions | 308192 308194 804826J2HU |
| Amoxicillin | AMOXICILLIN | NuCare Pharmaceuticals,Inc. | 7ee6b6b6-ae5b-2e39-e053-2991aa0a2377 | 2024-06-28 | Warnings, Adverse reactions | 308191 804826J2HU |
| Amoxicillin and Clavulanate Potassium | AMOXICILLIN AND CLAVULANATE POTASSIUM | A-S Medication Solutions | 46921419-9fae-4f51-b1b2-dc2e1ab04e8e | 2024-06-28 | Warnings, Adverse reactions | 804826J2HU |
| Amoxicillin | AMOXICILLIN | Asclemed USA, Inc. | 830bb8fb-3743-463a-9317-3f83e3e105ac | 2024-06-26 | Warnings, Adverse reactions | 308189 804826J2HU |
| Amoxicillin | AMOXICILLIN | NuCare Pharmaceuticals,Inc. | 997650f9-7eff-64de-e053-2995a90a617b | 2024-06-20 | Warnings, Adverse reactions | 308189 804826J2HU |
| Amoxicillin and Clavulanate Potassium | AMOXICILLIN AND CLAVULANATE POTASSIUM | NuCare Pharmaceuticals,Inc. | a0ff848d-230a-ab6b-e053-2a95a90a8bb8 | 2024-06-20 | Warnings, Adverse reactions | 804826J2HU |
| Amoxicillin | AMOXICILLIN | Aurobindo Pharma Limited | 99103779-6d2f-4e4b-9b7f-0b24d7c6bf4e | 2024-06-20 | Warnings, Adverse reactions | 308192 308194 804826J2HU |
| Amoxicillin and Clavulanate Potassium | AMOXICILLIN AND CLAVULANATE POTASSIUM | NuCare Pharmaceuticals,Inc. | 9263495c-310a-c20e-e053-2995a90a2e87 | 2024-06-19 | Warnings, Adverse reactions | 804826J2HU |
| Amoxicillin | AMOXICILLIN | NuCare Pharmaceuticals,Inc. | 97a657a3-8238-f5f1-e053-2a95a90a7a7a | 2024-06-19 | Warnings, Adverse reactions | 308189 804826J2HU |
| Amoxicillin | AMOXICILLIN | NuCare Pharmaceuticals,Inc. | 8c3ba9cf-9a28-3965-e053-2a95a90a38ce | 2024-06-18 | Warnings, Adverse reactions | 308182 804826J2HU |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.