NDC 71205-649 – Ciprofloxacin
Ciprofloxacin Hydrochloride 500 mg/1 · Tablet, Film Coated · Oral
Product NDC71205-649
Product details
- Brand name
- Ciprofloxacin
- Generic name
- Ciprofloxacin Hydrochloride
- Labeler
- Proficient Rx LP
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA077859
- Marketed since
- April 26, 2007
- Listing expires
- December 31, 2026
- Pharmacologic class
- Fluoroquinolone Antibacterial
Active ingredients
- Ciprofloxacin Hydrochloride 500 mg/1
Package NDC codes (7)
| Package NDC | Description | Since |
|---|---|---|
| 71205-649-06 | 6 TABLET, FILM COATED in 1 BOTTLE (71205-649-06) | Mar 28, 2022 |
| 71205-649-07 | 7 TABLET, FILM COATED in 1 BOTTLE (71205-649-07) | Jun 26, 2024 |
| 71205-649-10 | 10 TABLET, FILM COATED in 1 BOTTLE (71205-649-10) | Mar 28, 2022 |
| 71205-649-14 | 14 TABLET, FILM COATED in 1 BOTTLE (71205-649-14) | Mar 28, 2022 |
| 71205-649-20 | 20 TABLET, FILM COATED in 1 BOTTLE (71205-649-20) | Mar 28, 2022 |
| 71205-649-30 | 30 TABLET, FILM COATED in 1 BOTTLE (71205-649-30) | Mar 28, 2022 |
| 71205-649-60 | 60 TABLET, FILM COATED in 1 BOTTLE (71205-649-60) | Mar 28, 2022 |
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