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 |
|---|---|---|---|---|---|---|
| Wal Som Nighttime Sleep Aid | DIPHENHYDRAMINE HCL | Walgreens | ff475a69-dbb2-40a9-b7f4-9c7b7e975d19 | 2026-07-23 | Warnings | TC2D6JAD40 |
| Diphenhydramine Hydrochloride | DIPHENHYDRAMINE HYDROCHLORIDE | Sportpharm LLC | e5af2dd2-cc91-46c7-bdb9-97a7cdddcb69 | 2026-07-23 | Warnings, Adverse reactions | ANDA080817 TC2D6JAD40 |
| COLDTAC Plus | ACETAMINOPHEN, PHENYLEPHRIN HYDROCHLORIDE, DEXTROMETHORPHAN HYDROBROMIDE | OPMX LLC | 3496866c-682f-420b-bfdb-64ecebbf70a2 | 2026-07-23 | Warnings | 362O9ITL9D |
| CharmTex All in One Antibacterial Shave Gel Body Wash | BENZETHONIUM CHLORIDE | Yangzhou Jyr daily chemical Co., Ltd | 9c9bfc61-9504-4362-8bdb-c15aa66f5a06 | 2026-07-23 | Warnings | M003 PH41D05744 |
| Meridian Unwrapped Antibacterial Deodorant | BENZETHONIUM CHLORIDE | Yangzhou Jyr daily chemical Co., Ltd | d4d5cb95-5ee5-4006-b368-f3244fc9cd6c | 2026-07-23 | Warnings | M003 PH41D05744 |
| Meridian Antibacterial Deodorant | BENZETHONIUM CHLORIDE | Yangzhou Jyr daily chemical Co., Ltd | 8f10a193-7e01-40df-b62a-73fff5b830e3 | 2026-07-23 | Warnings | M003 PH41D05744 |
| MISTIFY WATERMELON HYDRATING HAND SANITIZER | ALCOHOL ANTISEPTIC | Kingkey MBC Life Technology Group Co.,Ltd | 574bf021-6352-e3fc-e063-6394a90ad6de | 2026-07-23 | Warnings | M003 3K9958V90M |
| FRESH THEORY ANTIBACTERIAL HAND WIPES - Vanilla, Strawberry, Fresh | BENZALKONIUM CHLORIDE | Quest USA Corp | 5719809b-1c74-4bf3-e063-6294a90ab008 | 2026-07-23 | Warnings | M003 1038558 F5UM2KM3W7 |
| Smart Care SUGAR COOKIE HAND SANITIZER | ETHYL ALCOHOL | Ashtel Studios Inc. | b7aac379-90d6-4039-9304-891056b40bc0 | 2026-07-22 | Warnings | 3K9958V90M |
| Cold and Flu Nighttime | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, TRIPROLIDINE HCL | CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED | 0ab2ba6a-1fac-4a34-ab76-0b50b425d0ba | 2026-07-22 | Warnings | 362O9ITL9D |
| True Coast SPF 50 Mineral Sunscreen | ZINC OXIDE 18%, TITANIUM DIOXIDE 6% | Foshan Sugar Max Cosmetics CO.,Ltd | 5379466d-8d14-5fc2-e063-6394a90abd7e | 2026-07-22 | Warnings | 15FIX9V2JP |
| TYLENOL COLD PLUS FLU MULTI-SYMPTOM GELS NIGHT | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE AND DOXYLAMINE SUCCINATE | Kenvue Brands LLC | 1c5386c1-e45d-9dcb-e063-6294a90aff07 | 2026-07-22 | Warnings | 362O9ITL9D |
| Tylenol Extra Strength | ACETAMINOPHEN | Kenvue Brands LLC | 103d109d-f520-409c-8da2-eb6b0fbec891 | 2026-07-22 | Warnings | 362O9ITL9D |
| Tylenol PM Extra Strength | ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE | Kenvue Brands LLC | ce58105b-f010-47af-8f31-6dd4ce4e9cba | 2026-07-22 | Warnings | TC2D6JAD40 362O9ITL9D |
| Droptics Dry Eye Relief | CARBOXYMETHYLCELLULOSE SODIUM,GLYCERIN,POLYSORBATE 80 | Droptics LLC | 29d7614b-f4b7-48e2-97c5-d1bff27731d2 | 2026-07-22 | Warnings | 6OZP39ZG8H |
| ALORYXA | GYNECOLOGICAL INTIMATE CARE GEL | Tupelo Brittany LLC | 57346a86-ab51-021a-e063-6394a90a1dc2 | 2026-07-22 | Warnings | 85H0HZU99M |
| First Aid Antiseptic | POVIDONE-IODINE 5% | Walgreen Company | 262ea2c8-f571-1c0b-e063-6394a90af20b | 2026-07-22 | Warnings | M003 85H0HZU99M |
| Allergy plus Sinus Headache | ACETAMINOPHEN 325 MG, DIPHENHYDRAMINE HCL 12.5 MG, PHENYLEPHRINE HCL 5 MG | Shield Pharmaceuticals Corp | 772d0184-8c41-40f1-bbef-7e68692eec66 | 2026-07-22 | Warnings | TC2D6JAD40 362O9ITL9D |
| Verifine Alcohol Swabs | ALCOHOL SWABS | Promisemed Hangzhou Meditech Co.,LTD. | 5738a502-c5ab-21b0-e063-6294a90a20a7 | 2026-07-22 | Warnings | M003 797544 ND2M416302 |
| KeepGoing Sting Relief Pad | BENZOCAINE AND ISOPROPYL ALCOHOL | J&A Digital Inc. | a630db1b-1674-4659-a60f-56994b0a1564 | 2026-07-22 | Warnings | M003 ND2M416302 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.