NDC 63323-280-01 - Furosemide
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
- 63323-280
- Requested NDC
- 63323-280-01
- Package NDCs from labels
- 63323-280-01, 63323-280-02, 63323-280-03, 63323-280-04, 63323-280-05, 63323-280-10, 63323-280-41, 63323-280-16, 63323-280-43, 63323-280-26, 63323-280-45, 63323-280-36
- Manufacturer
- Cardinal Health 107, LLC
- Effective date
- 2026-06-02
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Furosemide - Cardinal Health 107, LLC | Cardinal Health 107, LLC | 2026-06-02 | HUMAN PRESCRIPTION DRUG LABEL |
| Furosemide - Cardinal Health 107, LLC | Cardinal Health 107, LLC | 2025-10-03 | HUMAN PRESCRIPTION DRUG LABEL |
| Furosemide - Fresenius Kabi USA, LLC | Fresenius Kabi USA, LLC | 2024-12-09 | HUMAN PRESCRIPTION DRUG LABEL |
| Furosemide - Fresenius Kabi USA, LLC | Fresenius Kabi USA, LLC | 2024-12-09 | HUMAN PRESCRIPTION DRUG LABEL |
| FUROSEMIDE - HF Acquisition Co LLC, DBA HealthFirst | HF Acquisition Co LLC, DBA HealthFirst | 2024-01-28 | HUMAN PRESCRIPTION DRUG LABEL |
| FUROSEMIDE - HF Acquisition Co LLC, DBA HealthFirst | HF Acquisition Co LLC, DBA HealthFirst | 2024-01-22 | HUMAN PRESCRIPTION DRUG LABEL |
| FUROSEMIDE - HF Acquisition Co LLC, DBA HealthFirst | HF Acquisition Co LLC, DBA HealthFirst | 2021-06-28 | HUMAN PRESCRIPTION DRUG LABEL |
| Model AA-8565CV-ACT Model AA-8565CV - Aerospace Accessory Service, Inc | Aerospace Accessory Service, Inc | 2021-05-18 | MEDICAL DEVICE |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 63323-280-01 | Furosemide | 2 mL in 1 VIAL | INJECTION, SOLUTION | 2 | 6 | |
| 63323-280-02 | Furosemide | 25 in 1 TRAY | INJECTION, SOLUTION | 25 | 6 | |
| 63323-280-03 | Furosemide | 4 mL in 1 VIAL | INJECTION, SOLUTION | 4 | 6 | |
| 63323-280-04 | Furosemide | 25 in 1 TRAY | INJECTION, SOLUTION | 25 | 6 | |
| 63323-280-05 | Furosemide | 10 mL in 1 VIAL | INJECTION, SOLUTION | 10 | 6 | |
| 63323-280-10 | Furosemide | 25 in 1 TRAY | INJECTION, SOLUTION | 25 | 6 | |
| 63323-280-16 | Furosemide | 25 in 1 TRAY | INJECTION, SOLUTION | 25 | 5 | |
| 63323-280-26 | Furosemide | 25 in 1 TRAY | INJECTION, SOLUTION | 25 | 5 | |
| 63323-280-36 | Furosemide | 25 in 1 TRAY | INJECTION, SOLUTION | 25 | 5 | |
| 63323-280-41 | Furosemide | 2 mL in 1 VIAL | INJECTION, SOLUTION | 2 | 5 | |
| 63323-280-43 | Furosemide | 4 mL in 1 VIAL | INJECTION, SOLUTION | 4 | 5 | |
| 63323-280-45 | Furosemide | 10 mL in 1 VIAL | INJECTION, SOLUTION | 10 | 5 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 63323-280 | FUROSEMIDE INJECTION, SOLUTION [FRESENIUS KABI USA, LLC] | 6 | Current NDC, Legacy NDC, 6 package rows | 20241222_c794c95a-654e-48fe-9596-201fc122ff75.zip |
| 63323-280 | FUROSEMIDE INJECTION, SOLUTION [FRESENIUS KABI USA, LLC] | 5 | Current NDC, Legacy NDC, 6 package rows | 20241222_3747bbcd-783d-4baa-bb5b-b6827bf390e3.zip |
DailyMed Billing Units#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| FUROSEMIDE | ACTIVE INGREDIENT | 7LXU5N7ZO5 | FUROSEMIDE INJECTION, SOLUTION [APP PHARMACEUTICALS, LLC] | 1 | |
| FUROSEMIDE | ACTIVE MOIETY | 7LXU5N7ZO5 | FUROSEMIDE INJECTION, SOLUTION [APP PHARMACEUTICALS, LLC] | 1 | |
| HYDROCHLORIC ACID | INACTIVE INGREDIENT | QTT17582CB | FUROSEMIDE INJECTION, SOLUTION [APP PHARMACEUTICALS, LLC] | 1 | |
| SODIUM CHLORIDE | INACTIVE INGREDIENT | 451W47IQ8X | FUROSEMIDE INJECTION, SOLUTION [APP PHARMACEUTICALS, LLC] | 1 | |
| SODIUM HYDROXIDE | INACTIVE INGREDIENT | 55X04QC32I | FUROSEMIDE INJECTION, SOLUTION [APP PHARMACEUTICALS, LLC] | 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 |
|---|---|---|---|---|---|---|
| METOPROLOL TARTRATE | METOPROLOL TARTRATE | St. Mary's Medical Park Pharmacy | e55cd5b5-c739-24ba-e053-2995a90a3ed4 | 2026-06-01 | Warnings, Adverse reactions | 866511 W5S57Y3A5L |
| ACETAMINOPHEN AND CODEINE PHOSPHATE | ACETAMINOPHEN AND CODEINE PHOSPHATE | St. Mary's Medical Park Pharmacy | eac5f350-93e5-4dc2-e053-2a95a90aed60 | 2026-06-01 | Boxed warning, Warnings, Adverse reactions | 362O9ITL9D |
| WILD CHERRY HAND SANITIZING WIPES | HAND SANITIZING WIPES | Zhejiang Bright Care Co., Ltd | 54f8dca9-65d0-8cac-e063-6394a90a5813 | 2026-06-01 | Warnings | M003 1038558 F5UM2KM3W7 |
| MISTIFY WINTER BERRY HAND SANITIZER | ALCOHOL ANTISEPTIC | Kingkey MBC Life Technology Group Co.,Ltd | 552a96d0-bbe7-228b-e063-6294a90a41fb | 2026-06-01 | Warnings | M003 3K9958V90M |
| cookie glow hand sanitizer | ALCOHOL ANTISEPTIC | Kingkey MBC Life Technology Group Co.,Ltd | 552b129a-6ec2-9418-e063-6294a90a2d5e | 2026-06-01 | Warnings | M003 3K9958V90M |
| Vanilla Fleece Hand Sanitizer | ALCOHOL ANTISEPTIC | Kingkey MBC Life Technology Group Co.,Ltd | 552b83dd-3809-02e6-e063-6294a90a997f | 2026-06-01 | Warnings | M003 3K9958V90M |
| Berry Swirl Hand Sanitizer | ALCOHOL ANTISEPTIC | Kingkey MBC Life Technology Group Co.,Ltd | 552bc4ba-b9a9-4bea-e063-6394a90acfc0 | 2026-06-01 | Warnings | M003 3K9958V90M |
| BAJA BLAST HYDRATING HAND SANITIZER | ALCOHOL ANTISEPTIC | Kingkey MBC Life Technology Group Co.,Ltd | 552d9b48-34ed-8bb9-e063-6294a90a06c5 | 2026-06-01 | Warnings | M003 3K9958V90M |
| SHREK WAFFLE AND SSYRUP HAND SANITIZING WIPES | HAND SANITIZING WIPES | Zhejiang Bright Care Co., Ltd | 552d95ec-f61f-0a7c-e063-6394a90a929b | 2026-06-01 | Warnings | M003 1038558 F5UM2KM3W7 |
| MOUNTAIN DEW HYDRATING HAND SANITIZER | ALCOHOL ANTISEPTIC | Kingkey MBC Life Technology Group Co.,Ltd | 552e7850-248f-dbc2-e063-6394a90a9cfd | 2026-06-01 | Warnings | M003 3K9958V90M |
| CORE RED HYDRATING HAND SANITIZER | ALCOHOL ANTISEPTIC | Kingkey MBC Life Technology Group Co.,Ltd | 552e7850-2492-dbc2-e063-6394a90a9cfd | 2026-06-01 | Warnings | M003 3K9958V90M |
| PEPSI HYDRATING HAND SANITIZER | ALCOHOL ANTISEPTIC | Kingkey MBC Life Technology Group Co.,Ltd | 552e9e41-0573-94da-e063-6294a90aa8ec | 2026-06-01 | Warnings | M003 3K9958V90M |
| Visine Red Eye Hydrating Comfort Eye Drops | TETRAHYDROZOLINE HYDROCHLORIDE AND POLYETHYLENE GLYCOL 400 | Savings Distributors LLC | 558178eb-1eec-af0f-e063-6394a90afad9 | 2026-06-01 | Warnings | B697894SGQ |
| MISTIFY SWEET STRAWBERRY HAND SANITIZING WIPES | HAND SANITIZING WIPES | KING KEY MBC LIFE TECHNOLOGY GROUP CO., LTD | 55a00eb2-af6e-0ce9-e063-6394a90aa6f5 | 2026-06-01 | Warnings | M003 1038558 F5UM2KM3W7 |
| vanilla sugar hand sanitizer gel | ALCOHOL ANTISEPTIC | Kingkey MBC Life Technology Group Co.,Ltd | 567c99e6-3bc8-0600-e063-6294a90a94c9 | 2026-06-01 | Warnings | M003 3K9958V90M |
| SHREK GREEN APPLE HAND SANITIZING WIPES | HAND SANITIZING WIPES | Zhejiang Bright Care Co., Ltd | 567cbd30-c709-5f64-e063-6394a90adb92 | 2026-06-01 | Warnings | M003 1038558 F5UM2KM3W7 |
| very berry hand sanitizer gel | ALCOHOL ANTISEPTIC | Kingkey MBC Life Technology Group Co.,Ltd | 567d6ce2-59fa-01ae-e063-6394a90a9e78 | 2026-06-01 | Warnings | M003 3K9958V90M |
| SHERK WATERMELON HAND SANITIZER WIPES | HAND SANITIZING WIPES | Zhejiang Bright Care Co., Ltd | 567dbd8c-3af6-34b4-e063-6394a90a0e23 | 2026-06-01 | Warnings | M003 1038558 F5UM2KM3W7 |
| Extra Strength Acetaminophen | ACETAMINOPHEN | TIME CAP LABORATORIES, INC. | 58840cf4-aceb-c7cf-e063-6294a90a5ff4 | 2026-06-01 | Warnings | 362O9ITL9D |
| Cough and Runny Nose Childrens Plus | ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE | TOP CARE (Topco Associates LLC) | 6f04bd51-093c-4624-aef3-0145ac387386 | 2026-06-01 | Warnings | 362O9ITL9D |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.