NDC 80425-0493 – Ciprofloxacin Hydrochloride
Ciprofloxacin Hydrochloride 500 mg/1 · Tablet, Film Coated · Oral
Product NDC80425-0493
Product details
- Brand name
- Ciprofloxacin Hydrochloride
- Generic name
- Ciprofloxacin Hydrochloride
- Labeler
- Advanced Rx of Tennessee, LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076593
- Marketed since
- March 20, 2025
- Listing expires
- December 31, 2026
- Pharmacologic class
- Fluoroquinolone Antibacterial
Active ingredients
- Ciprofloxacin Hydrochloride 500 mg/1
Uses, dosage, side effects and warnings for Ciprofloxacin Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 80425-0493-1 | 20 TABLET, FILM COATED in 1 BOTTLE (80425-0493-1) | Mar 20, 2025 |
| 80425-0493-2 | 30 TABLET, FILM COATED in 1 BOTTLE (80425-0493-2) | Mar 20, 2025 |
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