NDC 0143-9928 – Ciprofloxacin
Ciprofloxacin Hydrochloride 500 mg/1 · Tablet, Film Coated · Oral
Product NDC0143-9928
Product details
- Brand name
- Ciprofloxacin
- Generic name
- Ciprofloxacin
- Labeler
- Hikma Pharmaceuticals USA Inc.
- 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 500 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 0143-9928-01 | 100 TABLET, FILM COATED in 1 BOTTLE (0143-9928-01) | Jun 9, 2004 |
| 0143-9928-05 | 500 TABLET, FILM COATED in 1 BOTTLE (0143-9928-05) | Jun 9, 2004 |
| 0143-9928-30 | 30 TABLET, FILM COATED in 1 BOTTLE (0143-9928-30) | Jun 9, 2004 |
Recalls mentioning this NDC
- D-220-2013 Apr 3, 2013 · Class II
Presence of Foreign Substance(s): A complaint was received for a rubber-like material in a 500 mg Ciprofloxacin tablet.
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