Furosemide
- Product NDC
- 70518-0809
- 11-digit product format
- 705180809
- Labeler code
- 70518
- Product ID
- 70518-0809_e26d9bff-9150-58e8-e053-2a95a90ae582
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- NDA018823
- Marketing category
- NDA
- Marketing start
- 2017-10-27
- 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 |
|---|
| 70518-0809-3 | 70518080903 | 30 TABLET in 1 BLISTER PACK (70518-0809-3) | 30 tablet | 2021-12-23 | 0000-00-00 | No | No | Current |