NDC 72162-1741 – Ciprofloxacin
Ciprofloxacin Hydrochloride 500 mg/1 · Tablet, Film Coated · Oral
Product NDC72162-1741
Product details
- Brand name
- Ciprofloxacin
- Generic name
- Ciprofloxacin Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076126
- Marketed since
- October 10, 2009
- Listing expires
- December 31, 2026
- Pharmacologic class
- Fluoroquinolone Antibacterial
Active ingredients
- Ciprofloxacin Hydrochloride 500 mg/1
Package NDC codes (8)
| Package NDC | Description | Since |
|---|---|---|
| 72162-1741-1 | 100 TABLET, FILM COATED in 1 BOTTLE (72162-1741-1) | Oct 4, 2024 |
| 72162-1741-2 | 14 TABLET, FILM COATED in 1 BOTTLE (72162-1741-2) | Oct 4, 2024 |
| 72162-1741-3 | 30 TABLET, FILM COATED in 1 BOTTLE (72162-1741-3) | Oct 4, 2024 |
| 72162-1741-4 | 20 TABLET, FILM COATED in 1 BOTTLE (72162-1741-4) | Oct 4, 2024 |
| 72162-1741-5 | 500 TABLET, FILM COATED in 1 BOTTLE (72162-1741-5) | Oct 4, 2024 |
| 72162-1741-6 | 60 TABLET, FILM COATED in 1 BOTTLE (72162-1741-6) | Oct 4, 2024 |
| 72162-1741-7 | 10 TABLET, FILM COATED in 1 BOTTLE (72162-1741-7) | Oct 4, 2024 |
| 72162-1741-8 | 120 TABLET, FILM COATED in 1 BOTTLE (72162-1741-8) | Oct 4, 2024 |
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