NDC 42708-088 – Ciprofloxacin
Ciprofloxacin Hydrochloride 500 mg/1 · Tablet, Film Coated · Oral
Product NDC42708-088
Product details
- Brand name
- Ciprofloxacin
- Generic name
- Ciprofloxacin
- Labeler
- QPharma Inc
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA077859
- Marketed since
- April 26, 2007
- Marketing end
- February 28, 2027
- Pharmacologic class
- Fluoroquinolone Antibacterial
Active ingredients
- Ciprofloxacin Hydrochloride 500 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 42708-088-14 sample | 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42708-088-14) | Jan 11, 2019 |
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