NDC 66104-8902 - V-Max
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
- 66104-8902
- Package NDCs from labels
- 66104-8902-2, 66104-8902-1, 66104-8902-3
- Manufacturer
- Phibro Animal Health
- Effective date
- 2023-11-08
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| V-Max - Phibro Animal Health | Phibro Animal Health | 2023-11-08 | VFD TYPE A MEDICATED ARTICLE ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 66104-8902-1 | V-Max | 25 kg in 1 BOX | POWDER | 25 | 8 | |
| 66104-8902-2 | V-Max | 45.3 kg in 1 DRUM | POWDER | 45.3 | 8 | |
| 66104-8902-3 | V-Max | 600 kg in 1 BAG | POWDER | 600 | 8 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 66104-8902 | V-MAX (VIRGINIAMYCIN) POWDER [PHIBRO ANIMAL HEALTH] | 8 | 3 package rows | 20231109_3674cacd-0d6f-4483-ab2c-2b53e5f65ae9.zip |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| VIRGINIAMYCIN | ACTIVE INGREDIENT | C49WS9N75L | V-MAX (VIRGINIAMYCIN) POWDER [PHIBRO ANIMAL HEALTH] | 4 | |
| VIRGINIAMYCIN | ACTIVE MOIETY | C49WS9N75L | V-MAX (VIRGINIAMYCIN) POWDER [PHIBRO ANIMAL HEALTH] | 4 | |
| CALCIUM CARBONATE | INACTIVE INGREDIENT | H0G9379FGK | V-MAX (VIRGINIAMYCIN) POWDER [PHIBRO ANIMAL HEALTH] | 4 | |
| CARBOXYMETHYLCELLULOSE SODIUM | INACTIVE INGREDIENT | K679OBS311 | V-MAX (VIRGINIAMYCIN) POWDER [PHIBRO ANIMAL HEALTH] | 4 | |
| MINERAL OIL | INACTIVE INGREDIENT | T5L8T28FGP | V-MAX (VIRGINIAMYCIN) POWDER [PHIBRO ANIMAL HEALTH] | 4 | |
| RICE BRAN | INACTIVE INGREDIENT | R60QEP13IC | V-MAX (VIRGINIAMYCIN) POWDER [PHIBRO ANIMAL HEALTH] | 4 | |
| SOYBEAN OIL | INACTIVE INGREDIENT | 241ATL177A | V-MAX (VIRGINIAMYCIN) POWDER [PHIBRO ANIMAL HEALTH] | 4 |
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 |
|---|---|---|---|---|---|---|
| Venexa FE | FERROUS FUMARATE, FOLIC ACID | PureTek Corporation | ba142128-21c4-4204-e053-2a95a90ae0d7 | 2023-01-11 | Warnings, Adverse reactions | H0G9379FGK |
| Ribotin-E | FERROUS FUMARATE, FOLIC ACID | PureTek Corporation | bb1492c5-bfcd-d632-e053-2a95a90ad7d1 | 2023-01-11 | Warnings, Adverse reactions | H0G9379FGK |
| Ventrixyl Fe | FERROUS FUMARATE, FOLIC ACID | PureTek Corporation | c7a626ec-88ec-d899-e053-2a95a90ab0ba | 2023-01-11 | Warnings, Adverse reactions | H0G9379FGK |
| Zintrexyl-C | FERROUS FUMARATE, FOLIC ACID | PureTek Corporation | bb1492c5-bfca-d632-e053-2a95a90ad7d1 | 2023-01-11 | Warnings, Adverse reactions | H0G9379FGK |
| EARACHE DROPS | BELLADONNA LEAF, CALCIUM CARBONATE, CHAMOMILE, LYCOPODIUM CLAVATUM SPORE, ANEMONE PATENS, AND SULFUR | Hyland's Inc. | 9b18453e-e338-4b8e-9856-85aca8c46ee1 | 2022-12-12 | Warnings | H0G9379FGK |
| Refresh Digital PF | CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN AND POLYSORBATE 80 | Allergan, Inc. | 97e83e68-6374-4df4-93f6-d707fc32748d | 2022-11-28 | Warnings | K679OBS311 |
| Refresh Digital | CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN, POLYSORBATE 80 | Allergan, Inc. | b2bd34d4-fab9-4f4b-9be2-5d30b55f5b81 | 2022-11-28 | Warnings | K679OBS311 |
| OSTEOBIOS | CALCITONIN HUMAN - CALCIUM CARBONATE - CALCIUM FLUORIDE - CALCIUM PHOSPHATE - ISOLEUCINE - LEUCINE - LYSINE - METHIONINE - PHENYLALANINE - SUS SCROFA BONE - SUS SCROFA PARATHYROID GLAND - THREONINE - TRYPTOPHAN - VALINE - | Guna spa | 1b8c8c83-1a46-4c0a-b883-e7dce781c5d1 | 2022-11-14 | Warnings | H0G9379FGK |
| REFRESH OPTIVE | CARBOXYMETHYLCELLULOSE SODIUM AND GLYCERIN | Allergan, Inc. | 7f8d88af-fd3b-4138-af61-f24c59ccebd7 | 2022-09-23 | Warnings | K679OBS311 |
| REFRESH OPTIVE Advanced | CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN, POLYSORBATE 80 | Allergan, Inc. | ebd0839e-2e1d-4e0e-986c-19f1f5c76358 | 2022-09-15 | Warnings | K679OBS311 |
| injoy heartburn relief | FAMOTIDINE, CALCIUM CARBONATE AND MAGNESIUM HYDROXIDE | L. Perrigo Company | aca1b9e5-a35e-4eef-b55a-4189cd1b2a02 | 2022-09-07 | Warnings | H0G9379FGK |
| REFRESH OPTIVE Advanced | CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN, AND POLYSORBATE 80 | Allergan, Inc. | aaa943e4-7c38-4c5a-b7c0-5a656d8cafc0 | 2022-09-01 | Warnings | K679OBS311 |
| Intralipid | I.V. FAT EMULSION | Baxter Healthcare CORP | 069460a5-3e9a-428f-b2dc-3405690f4fd7 | 2022-07-25 | Boxed warning, Adverse reactions | 241ATL177A |
| Intralipid | I.V. FAT EMULSION | Baxter Healthcare Corporation | 55609586-f0b4-42e6-8dd9-cd090afb5dca | 2022-07-21 | Boxed warning, Adverse reactions | 241ATL177A |
| Intralipid | I.V. FAT EMULSION | Baxter Healthcare Corporation | a69c82da-15ba-4d4d-8d7f-871dc3981eb8 | 2022-07-21 | Boxed warning, Adverse reactions | 241ATL177A |
| Intralipid | I. V. FAT EMULSION | Baxter Healthcare Corporation | dd269651-30e8-43f0-880f-484346eaafeb | 2022-07-21 | Boxed warning, Adverse reactions | 241ATL177A |
| signature care acid reducer complete | FAMOTIDINE, CALCIUM CARBONATE, MAGNESIUM HYDROXIDE | Safeway | 885f43ab-5c14-417b-aab7-e887dfc48f2e | 2022-07-20 | Warnings | H0G9379FGK |
| Dual Action Complete | FAMOTIDINE, CALCIUM CARBONATE AND MAGNESIUM HYDROXIDE | Kroger Company | 522a256b-a7c0-4783-bfff-3dc6b5a2b315 | 2022-07-12 | Warnings | H0G9379FGK |
| Equate Acid Reducer Complete | FAMOTIDINE, CALCIUM CARBONATE AND MAGNESIUM HYDROXIDE | Wal-Mart Stores Inc | 3400c3aa-15f2-4279-9623-72933298b3dd | 2022-07-12 | Warnings | H0G9379FGK |
| Basic Care Dual Action Complete | FAMOTIDINE, CALCIUM CARBONATE AND MAGNESIUM HYDROXIDE | Amazon.com Services LLC | 27235c87-2fe9-458f-8eb0-b9880199cd5a | 2022-07-11 | Warnings | H0G9379FGK |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.