NDC 51311-300 - Biomox
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
- 51311-300
- Package NDCs from labels
- 51311-300-15, 51311-300-30
- Manufacturer
- Virbac AH, Inc. | Medispray Laboratories Private Ltd | Centrient Pharmaceuticals Netherlands | Alcami Missouri Corporation | Alcami Carolinas Corporation
- Effective date
- 2022-01-05
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Approved by FDA under NADA # 065-495 BIOMOX® (amoxicillin) | Virbac AH, Inc. | Medispray Laboratories Private Ltd | Centrient Pharmaceuticals Netherlands | Alcami Missouri Corporation | Alcami Carolinas Corporation | 2022-01-05 | PRESCRIPTION ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 51311-300-15 | Biomox | 15 mL in 1 BOTTLE, DROPPER | SUSPENSION | 15 | 5 | |
| 51311-300-30 | Biomox | 30 mL in 1 BOTTLE, DROPPER | SUSPENSION | 30 | 5 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| amoxicillin | ACTIVE INGREDIENT | 804826J2HU | BIOMOX (AMOXICILLIN) SUSPENSION [VIRBAC AH, INC.] | 1 | |
| amoxicillin | ACTIVE MOIETY | 804826J2HU | BIOMOX (AMOXICILLIN) SUSPENSION [VIRBAC AH, INC.] | 1 |
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 | Coupler LLC | 5827b6de-6b48-d73a-e063-6394a90a4a72 | 2026-08-03 | Warnings, Adverse reactions | 804826J2HU |
| Amoxicillin | AMOXICILLIN | NuCare Pharmaceuticals,Inc. | 8cb987bf-d45a-c15a-e053-2995a90aad46 | 2026-08-03 | Warnings, Adverse reactions | 804826J2HU |
| Amoxicillin | AMOXICILLIN | Redpharm Drug | 57f5652d-ee50-eb7e-e063-6394a90a7b66 | 2026-08-01 | Warnings, Adverse reactions | 804826J2HU |
| Amoxicillin and Clavulanate Potassium | AMOXICILLIN AND CLAVULANATE POTASSIUM | Preferred Pharmaceuticals Inc. | 2c7a4de8-002a-472c-90d8-4c39a1f188c3 | 2026-07-31 | Warnings, Adverse reactions | 804826J2HU |
| Amoxicillin | AMOXICILLIN | Redpharm Drug | 57e56202-950b-10f6-e063-6394a90a4912 | 2026-07-31 | Warnings, Adverse reactions | 804826J2HU |
| Amoxicillin | AMOXICILLIN | NuCare Pharmaceuticals, Inc. | 4a402dba-c255-5db8-e054-00144ff8d46c | 2026-07-24 | Warnings, Adverse reactions | 804826J2HU |
| amoxicillin and clavulanate potassium | AMOXICILLIN AND CLAVULANATE POTASSIUM | Chartwell RX, LLC | 00b86913-50c8-443f-8467-f4f499d358af | 2026-07-23 | Warnings, Adverse reactions | 804826J2HU |
| Amoxicillin | AMOXICILLIN | REMEDYREPACK INC. | a2c91cf0-a4e4-44c0-b712-bee63dd6c22b | 2026-07-22 | Warnings, Adverse reactions | 804826J2HU |
| Amoxicillin | AMOXICILLIN | REMEDYREPACK INC. | 102c62ca-da20-4866-84a8-e3513824af4a | 2026-07-21 | Warnings, Adverse reactions | 804826J2HU |
| Amoxicillin | AMOXICILLIN | REMEDYREPACK INC. | 9618d038-e880-47f6-b8d7-bbf8ab35364d | 2026-07-21 | Warnings, Adverse reactions | 804826J2HU |
| 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 |
| AMOXICILLIN AND CLAVULANATE POTASSIUM | AMOXICILLIN AND CLAVULANATE POTASSIUM | REMEDYREPACK INC. | 6e1c6209-660f-4043-b6a6-eac5f7665ef9 | 2026-07-15 | Warnings, Adverse reactions | 804826J2HU |
| Amoxicillin | AMOXICILLIN | Preferred Pharmaceuticals Inc. | ad804b34-169c-44bf-a469-f1149433d96b | 2026-07-15 | Warnings, Adverse reactions | 804826J2HU |
| Amoxicillin and Clavulanate Potassium | AMOXICILLIN AND CLAVULANATE POTASSIUM | HAWAII REPACK, INC. | 7fb0f56e-c098-49e4-b075-2eb8936582aa | 2026-07-13 | Warnings, Adverse reactions | 804826J2HU |
| 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 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.