Furosemide
- Product NDC
- 70518-0836
- 11-digit product format
- 705180836
- Labeler code
- 70518
- Product ID
- 70518-0836_e2724be1-72d5-3d26-e053-2995a90a0d37
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- NDA018823
- Marketing category
- NDA
- Marketing start
- 2017-11-10
- 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
- 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 |
|---|
| 70518-0836-2 | 70518083602 | 30 TABLET in 1 BLISTER PACK (70518-0836-2) | 30 tablet | 2021-06-07 | 0000-00-00 | No | No | Current |