NDC 85534-0081 – Ciprofloxacin
Ciprofloxacin Hydrochloride 750 mg/1 · Tablet, Film Coated · Oral
Product NDC85534-0081
Product details
- Brand name
- Ciprofloxacin
- Generic name
- Ciprofloxacin Hydrochloride
- Labeler
- HAWAII REPACK, INC.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA077859
- Marketed since
- April 26, 2007
- Marketing end
- January 31, 2027
- Pharmacologic class
- Fluoroquinolone Antibacterial
Active ingredients
- Ciprofloxacin Hydrochloride 750 mg/1
Package NDC codes (7)
| Package NDC | Description | Since |
|---|---|---|
| 85534-0081-0 | 6 TABLET, FILM COATED in 1 BOTTLE (85534-0081-0) | Apr 26, 2007 |
| 85534-0081-1 | 10 TABLET, FILM COATED in 1 BOTTLE (85534-0081-1) | Apr 26, 2007 |
| 85534-0081-2 | 14 TABLET, FILM COATED in 1 BOTTLE (85534-0081-2) | Apr 26, 2007 |
| 85534-0081-3 | 20 TABLET, FILM COATED in 1 BOTTLE (85534-0081-3) | Apr 26, 2007 |
| 85534-0081-4 | 21 TABLET, FILM COATED in 1 BOTTLE (85534-0081-4) | Apr 26, 2007 |
| 85534-0081-5 | 28 TABLET, FILM COATED in 1 BOTTLE (85534-0081-5) | Apr 26, 2007 |
| 85534-0081-6 | 30 TABLET, FILM COATED in 1 BOTTLE (85534-0081-6) | Apr 26, 2007 |
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