NDC 13985-805 - CMPK
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
- 13985-805
- Package NDCs from labels
- 13985-805-50
- Manufacturer
- MWI (VetOne)
- Effective date
- 2026-03-20
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| CMPK - MWI (VetOne) | MWI (VetOne) | 2026-03-20 | PRESCRIPTION ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 13985-805-50 | CMPK | 500 mL in 1 BOTTLE, PLASTIC | INJECTION, SOLUTION | 500 | 4 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| Calcium Gluconate Monohydrate | ACTIVE INGREDIENT | CZN0MI5R31 | CMPK INJECTION, SOLUTION [MWI (VETONE)] | 2 | |
| Dextrose Monohydrate | ACTIVE INGREDIENT | LX22YL083G | CMPK INJECTION, SOLUTION [MWI (VETONE)] | 2 | |
| Magnesium Gluconate | ACTIVE INGREDIENT | T42NAD2KHC | CMPK INJECTION, SOLUTION [MWI (VETONE)] | 2 | |
| Potassium Chloride | ACTIVE INGREDIENT | 660YQ98I10 | CMPK INJECTION, SOLUTION [MWI (VETONE)] | 2 | |
| Sodium Hypophosphite Monohydrate | ACTIVE INGREDIENT | 4VN69WUP7N | CMPK INJECTION, SOLUTION [MWI (VETONE)] | 2 | |
| Calcium Cation | ACTIVE MOIETY | 2M83C4R6ZB | CMPK INJECTION, SOLUTION [MWI (VETONE)] | 2 | |
| Dextrose | ACTIVE MOIETY | IY9XDZ35W2 | CMPK INJECTION, SOLUTION [MWI (VETONE)] | 2 | |
| Magnesium cation | ACTIVE MOIETY | T6V3LHY838 | CMPK INJECTION, SOLUTION [MWI (VETONE)] | 2 | |
| Phosphorus | ACTIVE MOIETY | 27YLU75U4W | CMPK INJECTION, SOLUTION [MWI (VETONE)] | 2 | |
| Potassium cation | ACTIVE MOIETY | 295O53K152 | CMPK INJECTION, SOLUTION [MWI (VETONE)] | 2 |
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 |
|---|---|---|---|---|---|---|
| POTASSIUM CHLORIDE | POTASSIUM CHLORIDE | Aphena Pharma Solutions - Tennessee, LLC | 61fe55c2-fc9a-4fae-899a-06601baa78e1 | 2025-11-19 | Warnings, Adverse reactions | 660YQ98I10 |
| POTASSIUM CHLORIDE | POTASSIUM CHLORIDE | PD-Rx Pharmaceuticals, Inc. | 018fc687-1fba-202e-e063-6294a90a5c9a | 2025-11-17 | Warnings, Adverse reactions | 660YQ98I10 |
| Potassium Chloride | POTASSIUM CHLORIDE | BluePoint Laboratories | 3709ee9a-f885-4a75-ab51-36e9e1ef0427 | 2025-11-10 | Warnings, Adverse reactions | 660YQ98I10 |
| Potassium Chloride Extended-release | POTASSIUM CHLORIDE EXTENDED-RELEASE | Bluepoint Laboratories | d605ca36-2bfa-42cb-a46c-8ecb3162994e | 2025-11-10 | Warnings, Adverse reactions | 660YQ98I10 |
| LUMOe SKIN1 Skin Remedy | KALI MURIATICUM, PRUNUS SPINOSA, SILICEA, SARSAPARILLA | Applied Bioenergetics, LLC | d4d7fd2f-66bf-407d-ad36-2462e880b9f5 | 2025-11-10 | Warnings | 660YQ98I10 |
| LUMO Heal Seasonal Flu Companion | ARSENICUM ALBUM, EUPATORIUM PERFOLIATUM, KALI MURIATICUM, STICTA PULMONARIA | Applied Bioenergetics, LLC | da6b6258-f91e-4283-aeb2-54e7885a80b8 | 2025-11-10 | Warnings | 660YQ98I10 |
| Potassium Chloride | POTASSIUM CHLORIDE | Henry Schein, Inc. | 8367a2ae-dfd9-4515-838c-529920291ca0 | 2025-11-07 | Warnings, Adverse reactions | 660YQ98I10 |
| Potassium Chloride Extended-Release | POTASSIUM CHLORIDE | Bryant Ranch Prepack | 2feda15e-f325-41fe-a442-41a8cc62b855 | 2025-11-06 | Warnings, Adverse reactions | 660YQ98I10 |
| Potassium Chloride Extended-Release | POTASSIUM CHLORIDE | A-S Medication Solutions | d486f982-a7d3-463d-a68d-89365ddaf5bb | 2025-11-06 | Warnings, Adverse reactions | 660YQ98I10 |
| Potassium chloride | POTASSIUM CHLORIDE | A-S Medication Solutions | 4a2173ba-556b-4ad7-be81-4da79b739490 | 2025-11-06 | Warnings, Adverse reactions | 660YQ98I10 |
| Potassium Chloride Extended-release | POTASSIUM CHLORIDE EXTENDED-RELEASE | A-S Medication Solutions | de335131-bb8a-44e5-89fa-1478edbcdc0e | 2025-11-06 | Warnings, Adverse reactions | 660YQ98I10 |
| Potassium Chloride Extended-Release | POTASSIUM CHLORIDE | Bryant Ranch Prepack | 6fc9eef0-3dfc-4344-85c7-9f11d9b99b65 | 2025-11-06 | Warnings, Adverse reactions | 660YQ98I10 |
| Potassium Chloride Extended-release | POTASSIUM CHLORIDE EXTENDED-RELEASE | A-S Medication Solutions | edb6c987-e2c3-421f-8a8d-849c9e17ace8 | 2025-11-06 | Warnings, Adverse reactions | 660YQ98I10 |
| Potassium Chloride Extended-Release | POTASSIUM CHLORIDE | Bryant Ranch Prepack | 1b64b0c9-31a2-4ee7-8818-66de906ebeda | 2025-11-06 | Warnings, Adverse reactions | 660YQ98I10 |
| Lactated Ringers | SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, AND CALCIUM CHLORIDE | B. Braun Medical Inc. | d3d29c8f-c326-4097-814a-7f4e08c67068 | 2025-11-05 | Warnings, Adverse reactions | 660YQ98I10 |
| Ringers | SODIUM CHLORIDE, CALCIUM CHLORIDE, AND POTASSIUM CHLORIDE | B. Braun Medical Inc. | 01721071-af03-4894-95c1-10b8bc64b888 | 2025-11-05 | Warnings, Adverse reactions | 660YQ98I10 |
| Dextrose in Lactated Ringers | DEXTROSE, SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, AND CALCIUM CHLORIDE | B. Braun Medical Inc. | 190da07e-a616-46e6-b4e5-1c0ba39306e5 | 2025-11-05 | Warnings, Adverse reactions | 660YQ98I10 LX22YL083G |
| Potassium Chloride | POTASSIUM CHLORIDE | A-S Medication Solutions | 0ac9b8dc-0c8e-4cdc-ab9d-bd8cab4f4958 | 2025-11-05 | Warnings, Adverse reactions | 660YQ98I10 |
| Lactated Ringers | SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, AND CALCIUM CHLORIDE | B. Braun Medical Inc. | f6d82772-638c-4584-b9d3-8833669f5963 | 2025-11-05 | Warnings, Adverse reactions | 660YQ98I10 |
| Potassium chloride | POTASSIUM CHLORIDE | A-S Medication Solutions | eb6b608f-5e51-4bc9-8339-c5d5264cba98 | 2025-11-05 | Warnings, Adverse reactions | 660YQ98I10 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.