NDC 71335-1024 – Ciprofloxacin
Ciprofloxacin Hydrochloride 750 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-1024
Product details
- Brand name
- Ciprofloxacin
- Generic name
- Ciprofloxacin Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA077859
- Marketed since
- April 26, 2007
- Marketing end
- January 31, 2027
- Pharmacologic class
- Fluoroquinolone Antibacterial
Active ingredients
- Ciprofloxacin Hydrochloride 750 mg/1
Package NDC codes (7)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1024-1 | 20 TABLET, FILM COATED in 1 BOTTLE (71335-1024-1) | Dec 28, 2018 |
| 71335-1024-2 | 28 TABLET, FILM COATED in 1 BOTTLE (71335-1024-2) | Dec 28, 2021 |
| 71335-1024-3 | 14 TABLET, FILM COATED in 1 BOTTLE (71335-1024-3) | Dec 10, 2018 |
| 71335-1024-4 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-1024-4) | Dec 28, 2021 |
| 71335-1024-5 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-1024-5) | Dec 28, 2021 |
| 71335-1024-6 | 10 TABLET, FILM COATED in 1 BOTTLE (71335-1024-6) | Dec 11, 2018 |
| 71335-1024-7 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-1024-7) | Dec 28, 2021 |
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