Furosemide
- Product NDC
- 60760-708
- 11-digit product format
- 607600708
- Labeler code
- 60760
- Product ID
- 60760-708_7a8e69ee-6ae4-60e4-e053-2a91aa0af9a4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St Mary's Medical Park Pharmacy
- Application
- ANDA076796
- Marketing category
- ANDA
- Marketing start
- 2018-10-22
- 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
- 2020-12-31
- 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 |
|---|
| 60760-708-90 | 60760070890 | 90 TABLET in 1 BOTTLE, PLASTIC (60760-708-90) | 90 tablet | 2018-10-22 | 0000-00-00 | No | No | Current |