NDC 50090-7843 – Ciprofloxacin Hydrochloride
Ciprofloxacin Hydrochloride 500 mg/1 · Tablet, Film Coated · Oral
Product NDC50090-7843
Product details
- Brand name
- Ciprofloxacin Hydrochloride
- Generic name
- Ciprofloxacin Hydrochloride
- Labeler
- A-S Medication Solutions
- 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 (7)
| Package NDC | Description | Since |
|---|---|---|
| 50090-7843-0 | 20 TABLET, FILM COATED in 1 BOTTLE (50090-7843-0) | Dec 30, 2025 |
| 50090-7843-1 | 14 TABLET, FILM COATED in 1 BOTTLE (50090-7843-1) | Dec 30, 2025 |
| 50090-7843-3 | 6 TABLET, FILM COATED in 1 BOTTLE (50090-7843-3) | Dec 30, 2025 |
| 50090-7843-4 | 28 TABLET, FILM COATED in 1 BOTTLE (50090-7843-4) | Dec 30, 2025 |
| 50090-7843-5 | 10 TABLET, FILM COATED in 1 BOTTLE (50090-7843-5) | Dec 30, 2025 |
| 50090-7843-7 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-7843-7) | Dec 30, 2025 |
| 50090-7843-8 | 1 TABLET, FILM COATED in 1 BOTTLE (50090-7843-8) | Dec 30, 2025 |
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