Furosemide
- Product NDC
- 60760-217
- 11-digit product format
- 607600217
- Labeler code
- 60760
- Product ID
- 60760-217_f06e8d5d-24c3-80a1-e053-2995a90aa4a9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA077293
- Marketing category
- ANDA
- Marketing start
- 2017-12-14
- Marketing end
- 0000-00-00
- 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
- 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 |
|---|
| 60760-217-90 | 60760021790 | 90 TABLET in 1 BOTTLE, PLASTIC (60760-217-90) | 90 tablet | 2017-12-14 | 0000-00-00 | No | No | Current |