Furosemide
- Product NDC
- 50090-6221
- 11-digit product format
- 500906221
- Labeler code
- 50090
- Product ID
- 50090-6221_e5cddf5c-ef1f-4e7b-84b2-82bc7856fe24
- 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
- 2023-12-31
- 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 |
|---|
| 50090-6221-0 | 50090622100 | 33 BLISTER PACK in 1 BOX, UNIT-DOSE (50090-6221-0) > 1 TABLET in 1 BLISTER PACK | 33 blister pack | 2022-11-10 | 0000-00-00 | No | No | Current |