Furosemide
- Product NDC
- 0378-0216
- 11-digit product format
- 003780216
- Labeler code
- 0378
- Product ID
- 0378-0216_0d7d06e2-2804-4a02-b9d6-2f70d9d45c4e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Mylan Pharmaceuticals Inc.
- Application
- NDA018487
- Marketing category
- NDA
- Marketing start
- 1981-08-27
- 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
DailyMed Product Concepts#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0378-0216-01 | 00378021601 | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0216-01) | 100 tablet | 1981-08-27 | 0000-00-00 | No | No | Current |
| 0378-0216-10 | 00378021610 | 1000 TABLET in 1 BOTTLE, PLASTIC (0378-0216-10) | 1000 tablet | 1981-08-27 | 0000-00-00 | No | No | Current |