Furosemide
- Product NDC
- 63561-0164
- 11-digit product format
- 635610164
- Labeler code
- 63561
- Product ID
- 63561-0164_4870846b-dfe5-84bd-e063-6294a90aa56f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FUROSEMIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Granulation Technology, Inc.
- Application
- NDA018569
- Marketing category
- NDA
- Marketing start
- 2025-12-18
- Substance
- FUROSEMIDE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Increased Diuresis at Loop of Henle [PE], Loop Diuretic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Furosemide
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| FUROSEMIDE | 20 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 |
|---|
| 63561-0164-1 | Furosemide | 100 in 1 BOTTLE | TABLET | 100 | | 2 |
| 63561-0164-2 | Furosemide | 1000 in 1 BOTTLE | TABLET | 1000 | | 2 |
| 63561-0164-9 | Furosemide | 90 in 1 BOTTLE | TABLET | 90 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 63561-0164-1 | 63561016401 | 100 TABLET in 1 BOTTLE (63561-0164-1) | 100 tablet | 2026-01-15 | No | No | Current |
| 63561-0164-2 | 63561016402 | 1000 TABLET in 1 BOTTLE (63561-0164-2) | 1000 tablet | 2025-12-18 | No | No | Current |
| 63561-0164-9 | 63561016409 | 90 TABLET in 1 BOTTLE (63561-0164-9) | 90 tablet | 2025-12-18 | No | No | Current |