FUROSEMIDE
- Product NDC
- 61919-284
- 11-digit product format
- 619190284
- Labeler code
- 61919
- Product ID
- 61919-284_3fdcbef4-a7e0-4c52-e054-00144ff8d46c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FUROSEMIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- DIRECT RX
- Application
- ANDA076796
- Marketing category
- ANDA
- Marketing start
- 2014-01-01
- Marketing end
- 0000-00-00
- Substance
- FUROSEMIDE
- Active strength
- 40 mg/1
- Pharmacologic classes
- Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 61919-284-30 | FUROSEMIDE | 30 in 1 BOTTLE | TABLET | 30 | | 2 |
| 61919-284-90 | FUROSEMIDE | 90 in 1 BOTTLE | TABLET | 90 | | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-284 | FUROSEMIDE TABLET [DIRECT RX] | 2 | Legacy NDC, 2 package rows | 20161028_1d2a8ab4-48a1-47f9-8ac8-d04b100fcbd8.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 61919-284-30 | 61919028430 | 30 in 1 BOTTLE | Historical |
| 61919-284-90 | 61919028490 | 90 in 1 BOTTLE | Historical |