Furosemide
- Product NDC
- 70934-412
- 11-digit product format
- 709340412
- Labeler code
- 70934
- Product ID
- 70934-412_aefbf184-b37b-6249-e053-2a95a90a525d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. dba Northwind Pharmaceuticals
- Application
- NDA018823
- Marketing category
- NDA
- Marketing start
- 2019-07-18
- 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 |
|---|
| 70934-412-30 | 70934041230 | 30 TABLET in 1 BOTTLE, PLASTIC (70934-412-30) | 30 tablet | 2019-09-19 | 0000-00-00 | No | No | Current |
| 70934-412-90 | 70934041290 | 90 TABLET in 1 BOTTLE, PLASTIC (70934-412-90) | 90 tablet | 2019-07-18 | 0000-00-00 | No | No | Current |