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 |
|---|---|---|---|---|---|---|
| Amoxicillin and Clavulanate Potassium | AMOXICILLIN AND CLAVULANATE POTASSIUM | Sandoz Inc | e41387c8-2c74-4990-831f-64dc921ee138 | 2025-05-01 | Warnings, Adverse reactions | 804826J2HU |
| Amoxicillin and Clavulanate Potassium | AMOXICILLIN AND CLAVULANATE POTASSIUM | Sandoz Inc | 7cba82f0-9886-46e9-8dbd-43a448aade29 | 2025-05-01 | Warnings, Adverse reactions | 804826J2HU |
| Amoxicillin | AMOXICILLIN | PD-Rx Pharmaceuticals, Inc. | d37f2e3c-01f0-4a81-a46f-1615b82e2499 | 2025-04-17 | Warnings, Adverse reactions | 308182 804826J2HU |
| AMOXICILLIN | AMOXICILLIN | Redpharm Drug | 0a100e76-513c-98d3-e063-6294a90adf47 | 2025-04-09 | Warnings, Adverse reactions | 308191 804826J2HU |
| Amoxicillin | AMOXICILLIN | A-S Medication Solutions | e58a65d7-d813-446d-b70b-7465809a5d2c | 2025-04-09 | Warnings, Adverse reactions | 308191 804826J2HU |
| Amoxicillin | AMOXICILLIN | A-S Medication Solutions | 641ec2a8-368a-4c5c-8c11-37366a06ce93 | 2025-04-08 | Warnings, Adverse reactions | 308191 804826J2HU |
| Amoxicillin | AMOXICILLIN | A-S Medication Solutions | 9d56f34f-c025-4e97-8f5e-4d93f1ab0055 | 2025-04-08 | Warnings, Adverse reactions | 308191 804826J2HU |
| Amoxicillin and Clavulanate Potassium | AMOXICILLIN AND CLAVULANATE POTASSIUM | NorthStar Rx LLC | df4136c0-9efd-42c3-a487-e728e8b91275 | 2025-04-03 | Warnings, Adverse reactions | 804826J2HU |
| Amoxicillin | AMOXICILLIN | A-S Medication Solutions | 4b15c5b4-460c-449f-9e48-99870b382826 | 2025-04-02 | Warnings, Adverse reactions | 308191 804826J2HU |
| Amoxicillin and Clavulanate Potassium | AMOXICILLIN AND CLAVULANATE POTASSIUM | NuCare Pharmaceuticals, Inc. | 31d00820-1c20-d52b-e063-6394a90ac312 | 2025-04-02 | Warnings, Adverse reactions | 804826J2HU |
| Amoxicillin | AMOXICILLIN | Proficient Rx LP | 577d8a00-c538-4089-b788-01b4b92d22f2 | 2025-04-01 | Warnings, Adverse reactions | 308194 804826J2HU |
| Amoxicillin and Clavulanate Potassium | AMOXICILLIN AND CLAVULANATE POTASSIUM | Proficient Rx LP | b0d7eb3e-706a-482b-b106-9c137be55bb6 | 2025-04-01 | Warnings, Adverse reactions | 804826J2HU |
| Amoxicillin | AMOXICILLIN | NuCare Pharmaceuticals,Inc. | 54c1d2a4-fe96-6efb-e054-00144ff88e88 | 2025-03-31 | Warnings, Adverse reactions | 804826J2HU |
| Amoxicillin | AMOXICILLIN | Preferred Pharmaceuticals Inc. | 992d7829-34d1-4c88-8a5c-1a92d001d194 | 2025-03-24 | Warnings, Adverse reactions | 313850 804826J2HU |
| Amoxicillin and Clavulanate Potassium | AMOXICILLIN AND CLAVULANATE POTASSIUM | Devatis Inc. | a884cff6-bffd-41fd-904c-c694c995f338 | 2025-03-11 | Warnings, Adverse reactions | 804826J2HU |
| Amoxicillin and Clavulanate Potassium | AMOXICILLIN AND CLAVULANATE POTASSIUM | NuCare Pharmaceuticals, Inc. | 30144e2e-d336-8fa3-e063-6394a90a6068 | 2025-03-11 | Warnings, Adverse reactions | 804826J2HU |
| Addiclenz | ASPARTAME, BENZALKONIUM CHLORIDE, FORMALINUM, METHYLENE CHLORIDE, METHYLPARABEN, PROPYLPARABEN, SODIUM BENZOATE, SODIUM CITRATE, TITANIUM DIOXIDE, ZINCUM OXYDATUM, ARSENICUM ALBUM, BETA VULGARIS, BISPHENOL A, BOLDO, CHELIDONIUM MAJUS, COBALTUM METALLICUM, CUPRUM METALLICUM, GLYPHOSATE, IODIUM, LYCOPODIUM CLAVATUM, PETROSELINUM SATIVUM, PHOSPHORICUM ACIDUM, SELENIUM METALLICUM, TARAXACUM OFFICINALE, ZINCUM METALLICUM | Deseret Biologicals, Inc. | 25036c26-1c21-4e5a-b4db-b8e177458341 | 2025-03-11 | Warnings | Z0H242BBR1 |
| Amoxicillin and Clavulanate Potassium | AMOXICILLIN AND CLAVULANATE POTASSIUM | Devatis, Inc. | 90d0aa94-5c32-4fb7-8561-8763810d2847 | 2025-03-11 | Warnings, Adverse reactions | 804826J2HU |
| Amoxicillin | AMOXICILLIN | NuCare Pharmaceuticals, Inc. | 3d6cf1b3-f1dc-4eab-e054-00144ff88e88 | 2025-03-10 | Warnings, Adverse reactions | 598025 804826J2HU |
| amoxicillin and clavulanate potassium | AMOXICILLIN AND CLAVULANATE POTASSIUM | Devatis, Inc. | b0b2e164-e70d-471f-92ce-abdac6cb405f | 2025-03-10 | Warnings, Adverse reactions | 804826J2HU |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.