Furosemide
- Product NDC
- 72162-1361
- 11-digit product format
- 721621361
- Labeler code
- 72162
- Product ID
- 72162-1361_e959fd06-a804-409d-b545-bed5ba0f12ea
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076796
- Marketing category
- ANDA
- Marketing start
- 2004-03-26
- Substance
- FUROSEMIDE
- Active strength
- 40 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 | 40 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 7LXU5N7ZO5 |
| Rxcui | 313988 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-1361-0 | Furosemide | 1000 in 1 BOTTLE, PLASTIC | TABLET | 1000 | | 100 |
| 72162-1361-1 | Furosemide | 100 in 1 BOTTLE, PLASTIC | TABLET | 100 | | 100 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-1361 | FUROSEMIDE TABLET [BRYANT RANCH PREPACK] | 100 | Current NDC, 2 package rows | 20231005_020bc039-9e99-4895-96f8-0c6a556d3e67.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 |
|---|
| 72162-1361-0 | 72162136100 | 1000 TABLET in 1 BOTTLE, PLASTIC (72162-1361-0) | 1000 tablet | 2023-10-04 | No | No | Historical |
| 72162-1361-1 | 72162136101 | 100 TABLET in 1 BOTTLE, PLASTIC (72162-1361-1) | 100 tablet | 2023-10-04 | No | No | Historical |