Furosemide
- Product NDC
- 71610-284
- 11-digit product format
- 716100284
- Labeler code
- 71610
- Product ID
- 71610-284_ffdf5578-b8fa-4213-811d-a6701deca3ac
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- NDA018487
- Marketing category
- NDA
- Marketing start
- 1981-08-27
- Marketing end
- 0000-00-00
- 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
- 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 |
|---|
| 71610-284 | FUROSEMIDE TABLET [APHENA PHARMA SOLUTIONS - TENNESSEE, LLC] | 1 | Legacy NDC | 20190604_5b9d9ef6-d882-46a9-b63d-fb9c71a63018.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71610-284-53 | 71610028453 | 60 TABLET in 1 BOTTLE, PLASTIC (71610-284-53) | 60 tablet | 2019-05-29 | 0000-00-00 | No | No | Current |
| 71610-284-60 | 71610028460 | 90 TABLET in 1 BOTTLE, PLASTIC (71610-284-60) | 90 tablet | 2019-05-29 | 0000-00-00 | No | No | Current |
| 71610-284-80 | 71610028480 | 180 TABLET in 1 BOTTLE, PLASTIC (71610-284-80) | 180 tablet | 2019-05-29 | 0000-00-00 | No | No | Current |