FUROSEMIDE
- Product NDC
- 73043-024
- 11-digit product format
- 730430024
- Labeler code
- 73043
- Product ID
- 73043-024_3469f9cc-315f-4799-adab-08db8e4b388d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- furosemide
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Devatis Inc.
- Application
- ANDA215856
- Marketing category
- ANDA
- Marketing start
- 2024-08-10
- 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 |
|---|
| 73043-024-01 | FUROSEMIDE | 10 mL in 1 VIAL, GLASS | INJECTION, SOLUTION | 10 | | 3 |
| 73043-024-01 | FUROSEMIDE | 25 in 1 BOX | INJECTION, SOLUTION | 25 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 73043-024 | FUROSEMIDE INJECTION, SOLUTION [DEVATIS INC.] | 3 | Current NDC, 2 package rows | 20241108_c90bcb14-eb8d-4753-b339-3469c664ecd2.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 73043-024-01 | 73043002401 | 25 VIAL, GLASS in 1 BOX (73043-024-01) / 10 mL in 1 VIAL, GLASS | 2024-08-10 | No | No | Current |