Furosemide
- Product NDC
- 71335-0601
- 11-digit product format
- 713350601
- Labeler code
- 71335
- Product ID
- 71335-0601_1dcb0621-72e5-4104-bc93-b541f317f39b
- 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
- 2021-12-31
- 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 |
|---|
| 71335-0601-1 | 71335060101 | 30 TABLET in 1 BOTTLE (71335-0601-1) | 30 tablet | 2007-04-03 | 0000-00-00 | No | No | Current |
| 71335-0601-2 | 71335060102 | 90 TABLET in 1 BOTTLE (71335-0601-2) | 90 tablet | 2007-04-03 | 0000-00-00 | No | No | Current |
| 71335-0601-3 | 71335060103 | 60 TABLET in 1 BOTTLE (71335-0601-3) | 60 tablet | 2007-04-03 | 0000-00-00 | No | No | Current |
| 71335-0601-4 | 71335060104 | 100 TABLET in 1 BOTTLE (71335-0601-4) | 100 tablet | 2007-04-03 | 0000-00-00 | No | No | Current |
| 71335-0601-5 | 71335060105 | 7 TABLET in 1 BOTTLE (71335-0601-5) | 7 tablet | 2007-04-03 | 0000-00-00 | No | No | Current |
| 71335-0601-6 | 71335060106 | 28 TABLET in 1 BOTTLE (71335-0601-6) | 28 tablet | 2007-04-03 | 0000-00-00 | No | No | Current |
| 71335-0601-7 | 71335060107 | 14 TABLET in 1 BOTTLE (71335-0601-7) | 14 tablet | 2007-04-03 | 0000-00-00 | No | No | Current |
| 71335-0601-8 | 71335060108 | 10 TABLET in 1 BOTTLE (71335-0601-8) | 10 tablet | 2007-04-03 | 0000-00-00 | No | No | Current |
| 71335-0601-9 | 71335060109 | 20 TABLET in 1 BOTTLE (71335-0601-9) | 20 tablet | 2007-04-03 | 0000-00-00 | No | No | Current |