Furosemide
- Product NDC
- 0615-8370
- 11-digit product format
- 006158370
- Labeler code
- 0615
- Product ID
- 0615-8370_fb99ad62-fc5e-4eab-9f63-20246541729c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, LLC dba Vangard Labs
- Application
- ANDA076796
- Marketing category
- ANDA
- Marketing start
- 2004-03-26
- Substance
- FUROSEMIDE
- Active strength
- 80 mg/1
- 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 | 80 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 7LXU5N7ZO5 |
| Rxcui | 197732, 310429, 313988 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0615-8370-39 | Furosemide | 30 in 1 BLISTER PACK | TABLET | 30 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0615-8370 | FUROSEMIDE TABLET [NCS HEALTHCARE OF KY, LLC DBA VANGARD LABS] | 7 | Current NDC, Legacy NDC, 1 package rows | 20240919_114f4f4f-536a-4658-8fd0-2dd8c029b19a.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 |
|---|
| 0615-8370-39 | 00615837039 | 30 TABLET in 1 BLISTER PACK (0615-8370-39) | 30 tablet | 2020-12-15 | 0000-00-00 | No | No | Current |