Furosemide
- Product NDC
- 50090-2951
- 11-digit product format
- 500902951
- Labeler code
- 50090
- Product ID
- 50090-2951_61cbbcba-4d01-4581-a63c-e8bcfcc826e2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- NDA018823
- Marketing category
- NDA
- Marketing start
- 1983-11-10
- 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
- 2022-12-31
- 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 |
|---|
| 50090-2951-0 | 50090295100 | 33 BLISTER PACK in 1 BOX, UNIT-DOSE (50090-2951-0) > 1 TABLET in 1 BLISTER PACK | 33 blister pack | 2017-04-06 | 0000-00-00 | No | No | Current |