Furosemide
- Product NDC
- 55700-452
- 11-digit product format
- 557000452
- Labeler code
- 55700
- Product ID
- 55700-452_a5613d26-c9f1-4599-b175-06811c8728a5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-452-30 | 55700045230 | 30 TABLET in 1 BOTTLE (55700-452-30) | 30 tablet | 2016-11-11 | 0000-00-00 | No | No | Current |
| 55700-452-90 | 55700045290 | 90 TABLET in 1 BOTTLE (55700-452-90) | 90 tablet | 2017-01-20 | 0000-00-00 | No | No | Current |