NDC 71335-0852 – Furosemide
Furosemide 20 mg/1 · Tablet · Oral
Product NDC71335-0852
Product details
- Brand name
- Furosemide
- Generic name
- Furosemide
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA076796
- Marketed since
- March 26, 2004
- Listing expires
- December 31, 2026
- Pharmacologic class
- Loop Diuretic
Active ingredients
- Furosemide 20 mg/1
Package NDC codes (9)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0852-1 | 30 TABLET in 1 BOTTLE (71335-0852-1) | Jun 22, 2018 |
| 71335-0852-2 | 90 TABLET in 1 BOTTLE (71335-0852-2) | Jun 22, 2018 |
| 71335-0852-3 | 60 TABLET in 1 BOTTLE (71335-0852-3) | Jun 22, 2018 |
| 71335-0852-4 | 100 TABLET in 1 BOTTLE (71335-0852-4) | Jun 22, 2018 |
| 71335-0852-5 | 7 TABLET in 1 BOTTLE (71335-0852-5) | Jun 22, 2018 |
| 71335-0852-6 | 28 TABLET in 1 BOTTLE (71335-0852-6) | Jun 22, 2018 |
| 71335-0852-7 | 14 TABLET in 1 BOTTLE (71335-0852-7) | Jun 22, 2018 |
| 71335-0852-8 | 10 TABLET in 1 BOTTLE (71335-0852-8) | Jun 22, 2018 |
| 71335-0852-9 | 20 TABLET in 1 BOTTLE (71335-0852-9) | Jun 22, 2018 |
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