Furosemide
- Product NDC
- 43353-018
- 11-digit product format
- 433530018
- Labeler code
- 43353
- Product ID
- 43353-018_6b8291f1-dcbd-4c61-92a4-9b1d35eeecdc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA077293
- Marketing category
- ANDA
- Marketing start
- 2006-02-01
- 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
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 43353-018 | FUROSEMIDE (FUROSEMIDE) TABLET [APHENA PHARMA SOLUTIONS - TENNESSEE, LLC] | 1 | Legacy NDC | 20160708_f7aec34c-2373-483c-b89c-2c53320f3829.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43353-018-30 | 43353001830 | 30 TABLET in 1 BOTTLE (43353-018-30) | 30 tablet | 2015-04-07 | 0000-00-00 | No | No | Current |
| 43353-018-45 | 43353001845 | 45 TABLET in 1 BOTTLE (43353-018-45) | 45 tablet | 2015-04-07 | 0000-00-00 | No | No | Current |
| 43353-018-53 | 43353001853 | 60 TABLET in 1 BOTTLE (43353-018-53) | 60 tablet | 2015-04-07 | 0000-00-00 | No | No | Current |
| 43353-018-60 | 43353001860 | 90 TABLET in 1 BOTTLE (43353-018-60) | 90 tablet | 2015-04-07 | 0000-00-00 | No | No | Current |
| 43353-018-80 | 43353001880 | 180 TABLET in 1 BOTTLE (43353-018-80) | 180 tablet | 2015-04-07 | 0000-00-00 | No | No | Current |