NDC 69315-116 – Furosemide
Furosemide 20 mg/1 · Tablet · Oral
Product NDC69315-116
Product details
- Brand name
- Furosemide
- Generic name
- Furosemide
- Labeler
- Leading Pharma, LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA077293
- Marketed since
- February 1, 2006
- Listing expires
- December 31, 2026
- Pharmacologic class
- Loop Diuretic
Active ingredients
- Furosemide 20 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 69315-116-01 | 100 TABLET in 1 BOTTLE (69315-116-01) | May 15, 2016 |
| 69315-116-10 | 1000 TABLET in 1 BOTTLE (69315-116-10) | May 15, 2016 |
Recalls mentioning this NDC
- D-0486-2026 Apr 29, 2026 · Class II
CGMP Deviations; presence of N-nitroso-Furosemide (NNF) above the recommended intake limit.
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