Furosemide
- Product NDC
- 60760-707
- 11-digit product format
- 607600707
- Labeler code
- 60760
- Product ID
- 60760-707_b8b84751-ef69-2a28-e053-2995a90a8d79
- 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
- 2021-01-07
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60760-707 | FUROSEMIDE TABLET [ST. MARY'S MEDICAL PARK PHARMACY] | 1 | Legacy NDC | 20210113_b8b83a46-7de5-1f9c-e053-2995a90ac4ae.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-707-90 | 60760070790 | 90 TABLET in 1 BOTTLE, PLASTIC (60760-707-90) | 90 tablet | 2021-01-07 | 0000-00-00 | No | No | Current |