FUROSCIX
- Product NDC
- 71767-100
- 11-digit product format
- 717670100
- Labeler code
- 71767
- Product ID
- 71767-100_46518b53-5ca8-c68b-e063-6394a90a4150
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- furosemide injection 80 mg/ 10 mL
- Dosage form
- INJECTION
- Route
- SUBCUTANEOUS
- Labeler
- scPharmaceuticals Inc.
- Application
- NDA209988
- Marketing category
- NDA
- Marketing start
- 2022-11-14
- Substance
- FUROSEMIDE
- Active strength
- 8 mg/mL
- Pharmacologic classes
- Increased Diuresis at Loop of Henle [PE], Loop Diuretic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- FUROSCIX
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| FUROSEMIDE | 8 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 7LXU5N7ZO5 |
| Rxcui | 2621022, 2621028 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71767-100-01 | FUROSCIX | 1 in 1 KIT | INJECTION | 1 | | 18 |
| 71767-100-01 | FUROSCIX | 1 in 1 CARTON | INJECTION | 1 | | 18 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71767-100 | FUROSCIX (FUROSEMIDE INJECTION 80 MG/ 10 ML) INJECTION [SCPHARMACEUTICALS INC.] | 16 | Current NDC, Legacy NDC, 2 package rows | 20250315_eac958dd-8d43-e44e-e053-2995a90a4d5e.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71767-100-01 | 71767010001 | 1 CARTON in 1 KIT (71767-100-01) / 1 CARTRIDGE in 1 CARTON / 10 mL in 1 CARTRIDGE | 1 carton | 2022-11-14 | 0000-00-00 | No | No | Current |