Furosemide
- Product NDC
- 43063-806
- 11-digit product format
- 430630806
- Labeler code
- 43063
- Product ID
- 43063-806_e6d7054b-a8c9-196c-e053-2a95a90a60bd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- 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
- 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 |
|---|
| 43063-806-21 | 43063080621 | 21 TABLET in 1 BOTTLE, PLASTIC (43063-806-21) | 21 tablet | 2017-12-04 | 0000-00-00 | No | No | Current |
| 43063-806-30 | 43063080630 | 30 TABLET in 1 BOTTLE, PLASTIC (43063-806-30) | 30 tablet | 2017-12-01 | 0000-00-00 | No | No | Current |
| 43063-806-90 | 43063080690 | 90 TABLET in 1 BOTTLE, PLASTIC (43063-806-90) | 90 tablet | 2018-01-16 | 0000-00-00 | No | No | Current |