Furosemide
- Product NDC
- 43063-849
- 11-digit product format
- 430630849
- Labeler code
- 43063
- Product ID
- 43063-849_39fd20b5-22d0-8252-e063-6294a90adaad
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA076796
- Marketing category
- ANDA
- Marketing start
- 2004-03-26
- 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
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 7LXU5N7ZO5 | FUROSEMIDE | 54-31-9 | FUROSEMIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 43063-849-21 | 43063084921 | 21 TABLET in 1 BOTTLE, PLASTIC (43063-849-21) | 21 tablet | 2018-04-27 | No | No | Historical |
| 43063-849-30 | 43063084930 | 30 TABLET in 1 BOTTLE, PLASTIC (43063-849-30) | 30 tablet | 2018-04-27 | No | No | Historical |
| 43063-849-60 | 43063084960 | 60 TABLET in 1 BOTTLE, PLASTIC (43063-849-60) | 60 tablet | 2018-05-03 | No | No | Historical |
| 43063-849-90 | 43063084990 | 90 TABLET in 1 BOTTLE, PLASTIC (43063-849-90) | 90 tablet | 2018-05-03 | No | No | Historical |