Furosemide
- Product NDC
- 0615-7957
- 11-digit product format
- 006157957
- Labeler code
- 0615
- Product ID
- 0615-7957_8676925e-cabd-4690-9632-afed4b1211c9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Application
- ANDA070086
- Marketing category
- ANDA
- Marketing start
- 1991-03-13
- Marketing end
- 2022-09-30
- Substance
- FUROSEMIDE
- Active strength
- 80 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 |
|---|
| 0615-7957-39 | 00615795739 | 30 TABLET in 1 BLISTER PACK (0615-7957-39) | 30 tablet | 2016-04-04 | 2022-09-30 | No | No | Current |