NDC 82804-260 – Ciprofloxacin Hydrochloride
Ciprofloxacin Hydrochloride 500 mg/1 · Tablet, Film Coated · Oral
Product NDC82804-260
Product details
- Brand name
- Ciprofloxacin Hydrochloride
- Generic name
- Ciprofloxacin Hydrochloride
- Labeler
- Proficient Rx LP
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076593
- Marketed since
- May 23, 2024
- Listing expires
- December 31, 2027
- Pharmacologic class
- Fluoroquinolone Antibacterial
Active ingredients
- Ciprofloxacin Hydrochloride 500 mg/1
Uses, dosage, side effects and warnings for Ciprofloxacin Hydrochloride →
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 82804-260-06 | 6 TABLET, FILM COATED in 1 BOTTLE (82804-260-06) | Jun 1, 2026 |
| 82804-260-07 | 7 TABLET, FILM COATED in 1 BOTTLE (82804-260-07) | Apr 20, 2026 |
| 82804-260-10 | 10 TABLET, FILM COATED in 1 BOTTLE (82804-260-10) | Mar 12, 2026 |
| 82804-260-14 | 14 TABLET, FILM COATED in 1 BOTTLE (82804-260-14) | Dec 30, 2025 |
| 82804-260-20 | 20 TABLET, FILM COATED in 1 BOTTLE (82804-260-20) | Dec 30, 2025 |
| 82804-260-30 | 30 TABLET, FILM COATED in 1 BOTTLE (82804-260-30) | Aug 4, 2026 |
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