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 | AMOXICILLIN | A-S Medication Solutions | 8bac30bb-1dbc-41de-ad50-0a1883f96198 | 2023-11-17 | Warnings, Adverse reactions | 804826J2HU |
| Amoxicillin and Clavulanate Potassium | AMOXICILLIN AND CLAVULANATE POTASSIUM | A-S Medication Solutions | 61f9224b-a91b-4154-a7f3-22c14601230f | 2023-10-31 | Warnings, Adverse reactions | 804826J2HU |
| Amoxicillin and Clavulanate Potassium | AMOXICILLIN AND CLAVULANATE POTASSIUM | Proficient Rx LP | e05caabb-b95c-4e54-890e-bbc371a20fc3 | 2023-10-01 | Warnings, Adverse reactions | 804826J2HU |
| Amoxicillin | AMOXICILLIN | A-S Medication Solutions | 156ef8e9-b6e4-4512-865f-7139c90c8f9b | 2023-09-10 | Warnings, Adverse reactions | 308189 804826J2HU |
| Amoxicillin and Clavulanate Potassium | AMOXICILLIN AND CLAVULANATE POTASSIUM | Asclemed USA, Inc. | f14a8008-c0ff-4628-af99-e5f07b19df71 | 2023-09-06 | Warnings, Adverse reactions | 804826J2HU |
| Amoxicillin and Clavulanate Potassium | AMOXICILLIN AND CLAVULANATE POTASSIUM | Asclemed USA, Inc. | 8c4125d4-d074-40d4-9def-d3a528fc8c8e | 2023-09-06 | Warnings, Adverse reactions | 804826J2HU |
| Lipotox | SQUALENE, CHOLESTERINUM, ESTRADIOL, PROGESTERONE, ASPARTAME, BENZALKONIUM CHLORIDE, FORMALINUM, METHYLENE CHLORIDE, METHYLPARABEN, PROPYLPARABEN, SODIUM BENZOATE, SODIUM CITRATE, TITANIUM DIOXIDE, ZINCUM OXYDATUM, ARSENICUM ALBUM, LYCOPODIUM CLAVATUM, NUX VOMICA, PHOSPHORICUM ACIDUM, PHOSPHORUS, ACETICUM ACIDUM, BENZOICUM ACIDUM, BENZYL ALCOHOL, BORICUM ACIDUM, CHLORINUM, CORTISONE ACETICUM, EUGENOL, FOLLICULINUM, ISOPROPYL PALMITATE, LACTICUM ACIDUM, PETROLEUM JELLY, PHENYL BUTAZONE, PLUMBUM METALLICUM, | BioActive Nutritional, Inc. | a1538692-ca00-4e52-9b7e-409767ee27e1 | 2023-09-05 | Warnings | Z0H242BBR1 |
| Mannitol | MANNITOL | B. Braun Medical Inc. | d12cc802-b538-4065-a264-f474ff3b3043 | 2023-08-15 | Warnings, Adverse reactions | 3OWL53L36A |
| Amoxicillin | AMOXICILLIN | Proficient Rx LP | 2c395111-c9c1-483e-a542-58b935ede689 | 2023-08-01 | Warnings, Adverse reactions | 308191 804826J2HU |
| Amoxicillin | AMOXICILLIN | Asclemed USA, Inc. | bfd67724-fb22-4eac-8ebd-555614c16329 | 2023-06-17 | Warnings, Adverse reactions | 804826J2HU |
| Amoxicillin | AMOXICILLIN | Bryant Ranch Prepack | c5d39ce2-8ae4-4bba-893f-a713afba1893 | 2023-04-17 | Warnings, Adverse reactions | 308194 308191 804826J2HU |
| Amoxicillin | AMOXICILLIN | Asclemed USA, Inc. | be1d1a44-7ef3-445d-9970-494921de4c9d | 2023-03-18 | Warnings, Adverse reactions | 308191 804826J2HU |
| Mannitol | MANNITOL | Fresenius Kabi USA, LLC | c395e13d-6ea1-4104-8b37-669cfb982f04 | 2023-03-16 | Warnings, Adverse reactions | 3OWL53L36A |
| Amoxicillin and Clavulanate Potassium | AMOXICILLIN AND CLAVULANATE POTASSIUM | A-S Medication Solutions | 029a49f2-2132-4160-a0d6-2d108a456a22 | 2023-03-02 | Warnings, Adverse reactions | 804826J2HU |
| Amoxicillin | AMOXICILLIN | Proficient Rx LP | d5eba477-e255-4d97-9e16-30543c298680 | 2023-03-01 | Warnings, Adverse reactions | 313850 804826J2HU |
| Amoxicillin | AMOXICILLIN | A-S Medication Solutions | 77265bcd-c05d-443a-84c4-6e5ac75ee42c | 2023-02-21 | Warnings, Adverse reactions | 308189 804826J2HU |
| Amoxicillin | AMOXICILLIN | A-S Medication Solutions | 6c7bccff-00bf-46b0-a9ee-eb27d38d7377 | 2023-02-04 | Warnings, Adverse reactions | 804826J2HU |
| Amoxicillin and Clavulanate Potassium | AMOXICILLIN AND CLAVULANATE POTASSIUM | Asclemed USA, Inc. | f05a27dd-5ced-4f62-8a0c-548c3a033f5e | 2022-12-13 | Warnings, Adverse reactions | 804826J2HU |
| Amoxicillin | AMOXICILLIN | Asclemed USA, Inc. | fe9e12de-9be9-4211-9a58-c7ecd9e838d5 | 2022-11-02 | Warnings, Adverse reactions | 308191 804826J2HU |
| Amoxicillin and Clavulanate Potassium | AMOXICILLIN AND CLAVULANATE POTASSIUM | Proficient Rx LP | a0d22635-0e11-448d-b151-6f6168c65723 | 2022-11-01 | Warnings, Adverse reactions | 804826J2HU |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.