Furosemide
- Product NDC
- 55154-5540
- 11-digit product format
- 551545540
- Labeler code
- 55154
- Product ID
- 55154-5540_9b0718ed-4e0b-4f46-a08c-eb48b414a459
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Cardinal Health 107, LLC
- Application
- NDA018487
- Marketing category
- NDA
- Marketing start
- 2010-10-12
- Marketing end
- 2030-01-31
- 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
- 0000-00-00
- 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 |
|---|
| 55154-5540-0 | 55154554000 | 10 BLISTER PACK in 1 BAG (55154-5540-0) > 1 TABLET in 1 BLISTER PACK | 10 blister pack | 2010-10-12 | 2030-01-31 | No | No | Current |