NDC 63629-3868 – Ciprofloxacin
Ciprofloxacin Hydrochloride 750 mg/1 · Tablet, Film Coated · Oral
Product NDC63629-3868
Product details
- Brand name
- Ciprofloxacin
- Generic name
- Ciprofloxacin
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076558
- Marketed since
- June 9, 2004
- Listing expires
- December 31, 2026
- Pharmacologic class
- Fluoroquinolone Antibacterial
Active ingredients
- Ciprofloxacin Hydrochloride 750 mg/1
Package NDC codes (7)
| Package NDC | Description | Since |
|---|---|---|
| 63629-3868-1 | 20 TABLET, FILM COATED in 1 BOTTLE (63629-3868-1) | Oct 30, 2008 |
| 63629-3868-2 | 28 TABLET, FILM COATED in 1 BOTTLE (63629-3868-2) | Jun 12, 2009 |
| 63629-3868-3 | 14 TABLET, FILM COATED in 1 BOTTLE (63629-3868-3) | Apr 23, 2013 |
| 63629-3868-4 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-3868-4) | Jul 26, 2011 |
| 63629-3868-5 | 60 TABLET, FILM COATED in 1 BOTTLE (63629-3868-5) | Dec 14, 2010 |
| 63629-3868-6 | 10 TABLET, FILM COATED in 1 BOTTLE (63629-3868-6) | Dec 3, 2013 |
| 63629-3868-7 | 90 TABLET, FILM COATED in 1 BOTTLE (63629-3868-7) | Mar 6, 2023 |
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