FUROSEMIDE
- Product NDC
- 70518-4444
- 11-digit product format
- 705184444
- Labeler code
- 70518
- Product ID
- 70518-4444_3c69d295-cb49-1d42-e063-6394a90a63ba
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- furosemide
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA202747
- Marketing category
- ANDA
- Marketing start
- 2025-08-15
- 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 |
|---|
| 70518-4444-0 | FUROSEMIDE | 25 in 1 BOX | INJECTION, SOLUTION | 25 | | 1 |
| 70518-4444-1 | FUROSEMIDE | 4 mL in 1 VIAL, GLASS | INJECTION, SOLUTION | 4 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70518-4444-0 | 70518444400 | 25 VIAL, GLASS in 1 BOX (70518-4444-0) / 4 mL in 1 VIAL, GLASS (70518-4444-1) | | 2025-08-15 | No | No | Historical |
| 70518-4444-1 | 70518444401 | 4 mL in 1 VIAL, GLASS | 4 ml | | | | Historical |