NDC 71335-2450 – Ciprofloxacin
Ciprofloxacin Hydrochloride 500 mg/1 · Tablet · Oral
Product NDC71335-2450
Product details
- Brand name
- Ciprofloxacin
- Generic name
- Ciprofolxacin
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA208921
- Marketed since
- October 1, 2023
- Listing expires
- December 31, 2026
- Pharmacologic class
- Fluoroquinolone Antibacterial
Active ingredients
- Ciprofloxacin Hydrochloride 500 mg/1
Package NDC codes (10)
| Package NDC | Description | Since |
|---|---|---|
| 71335-2450-0 | 7 TABLET in 1 BOTTLE (71335-2450-0) | Aug 15, 2024 |
| 71335-2450-1 | 14 TABLET in 1 BOTTLE (71335-2450-1) | Aug 15, 2024 |
| 71335-2450-2 | 30 TABLET in 1 BOTTLE (71335-2450-2) | Aug 15, 2024 |
| 71335-2450-3 | 20 TABLET in 1 BOTTLE (71335-2450-3) | Aug 15, 2024 |
| 71335-2450-4 | 60 TABLET in 1 BOTTLE (71335-2450-4) | Aug 15, 2024 |
| 71335-2450-5 | 6 TABLET in 1 BOTTLE (71335-2450-5) | Aug 15, 2024 |
| 71335-2450-6 | 10 TABLET in 1 BOTTLE (71335-2450-6) | Aug 15, 2024 |
| 71335-2450-7 | 28 TABLET in 1 BOTTLE (71335-2450-7) | Aug 15, 2024 |
| 71335-2450-8 | 100 TABLET in 1 BOTTLE (71335-2450-8) | Aug 15, 2024 |
| 71335-2450-9 | 40 TABLET in 1 BOTTLE (71335-2450-9) | Aug 15, 2024 |
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