Furosemide
- Product NDC
- 72603-133
- 11-digit product format
- 726030133
- Labeler code
- 72603
- Product ID
- 72603-133_ad1cb298-ee74-429e-81e5-82eb2e6bfd77
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- NorthStar Rx LLC
- Application
- ANDA203428
- Marketing category
- ANDA
- Marketing start
- 2023-02-01
- 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 | 1719286, 1719290, 1719291 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72603-133-01 | Furosemide | 2 mL in 1 VIAL | INJECTION, SOLUTION | 2 | | 4 |
| 72603-133-25 | Furosemide | 25 in 1 CARTON | INJECTION, SOLUTION | 25 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72603-133 | FUROSEMIDE INJECTION, SOLUTION [NORTHSTAR RX LLC] | 3 | Current NDC, 2 package rows | 20250501_fc3194a3-7e75-4551-8334-4a5cc22d9f8b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72603-133-01 | 72603013301 | 2 mL in 1 VIAL | 2 ml | | | | Historical |
| 72603-133-25 | 72603013325 | 25 VIAL in 1 CARTON (72603-133-25) / 2 mL in 1 VIAL (72603-133-01) | 25 vial | 2023-02-01 | No | No | Current |