Furosemide
- Product NDC
- 63629-8057
- 11-digit product format
- 636298057
- Labeler code
- 63629
- Product ID
- 63629-8057_e06e8a67-7f12-487c-8690-2c9d2f05884a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-8057-1 | 63629805701 | 30 TABLET in 1 BOTTLE (63629-8057-1) | 30 tablet | 2019-08-26 | 0000-00-00 | No | No | Current |
| 63629-8057-2 | 63629805702 | 90 TABLET in 1 BOTTLE (63629-8057-2) | 90 tablet | 2019-08-26 | 0000-00-00 | No | No | Current |