FUROSEMIDE
- Product NDC
- 72572-190
- 11-digit product format
- 725720190
- Labeler code
- 72572
- Product ID
- 72572-190_4e63826f-f7be-4cc6-b21d-03aec09b9c5e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- furosemide
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Civica, Inc.
- Application
- ANDA202747
- Marketing category
- ANDA
- Marketing start
- 2022-09-23
- Substance
- FUROSEMIDE
- Active strength
- 10 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
- FUROSEMIDE
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| FUROSEMIDE | 10 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 7LXU5N7ZO5 |
| Rxcui | 1719291 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72572-190-25 | FUROSEMIDE | 4 mL in 1 VIAL, SINGLE-DOSE | INJECTION, SOLUTION | 4 | | 4 |
| 72572-190-25 | FUROSEMIDE | 25 in 1 BOX | INJECTION, SOLUTION | 25 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72572-190 | FUROSEMIDE INJECTION, SOLUTION [CIVICA, INC.] | 3 | Current NDC, Legacy NDC, 2 package rows | 20241109_7ecaa5af-d186-4380-b105-e7e528f75cc7.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72572-190-25 | 72572019025 | 25 VIAL, SINGLE-DOSE in 1 BOX (72572-190-25) / 4 mL in 1 VIAL, SINGLE-DOSE | 2022-09-23 | 0000-00-00 | No | No | Current |