NDC 16252-515 – Ciprofloxacin
Ciprofloxacin Hydrochloride 500 mg/1 · Tablet, Film Coated · Oral
Product NDC16252-515
Product details
- Brand name
- Ciprofloxacin
- Generic name
- Ciprofloxacin
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076794
- Marketed since
- November 1, 2006
- Marketing end
- August 31, 2027
- Pharmacologic class
- Fluoroquinolone Antibacterial
Active ingredients
- Ciprofloxacin Hydrochloride 500 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 16252-515-01 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16252-515-01) | Nov 1, 2006 |
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