Furosemide
- Product NDC
- 0615-7937
- 11-digit product format
- 006157937
- Labeler code
- 0615
- Product ID
- 0615-7937_60b20d21-dcbb-47e5-b58a-2011e2b0b849
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Application
- NDA018823
- Marketing category
- NDA
- Marketing start
- 1983-11-10
- Marketing end
- 2022-09-30
- 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
- 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 |
|---|
| 0615-7937-05 | 00615793705 | 15 TABLET in 1 BLISTER PACK (0615-7937-05) | 15 tablet | 2018-07-03 | 2022-09-30 | No | No | Current |
| 0615-7937-07 | 00615793707 | 7 TABLET in 1 BLISTER PACK (0615-7937-07) | 7 tablet | 2018-07-03 | 2022-09-30 | No | No | Current |
| 0615-7937-14 | 00615793714 | 14 TABLET in 1 BLISTER PACK (0615-7937-14) | 14 tablet | 2018-07-03 | 2022-09-30 | No | No | Current |
| 0615-7937-28 | 00615793728 | 28 TABLET in 1 BLISTER PACK (0615-7937-28) | 28 tablet | 2018-07-06 | 2022-09-30 | No | No | Current |
| 0615-7937-30 | 00615793730 | 6 BLISTER PACK in 1 BOX, UNIT-DOSE (0615-7937-30) > 5 TABLET in 1 BLISTER PACK | 6 blister pack | 2019-11-21 | 2022-09-30 | No | No | Current |
| 0615-7937-39 | 00615793739 | 30 TABLET in 1 BLISTER PACK (0615-7937-39) | 30 tablet | 2018-07-03 | 2022-09-30 | No | No | Current |