Furosemide
- Product NDC
- 63629-8058
- 11-digit product format
- 636298058
- Labeler code
- 63629
- Product ID
- 63629-8058_33f8e109-3cfa-458c-96c8-ad6528aa9390
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076796
- Marketing category
- ANDA
- Marketing start
- 2004-03-26
- 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 |
|---|
| 63629-8058-1 | 63629805801 | 30 TABLET in 1 BOTTLE (63629-8058-1) | 30 tablet | 2019-07-15 | 0000-00-00 | No | No | Current |