NDC 72789-511 – Ciprofloxacin
Ciprofloxacin Hydrochloride 500 mg/1 · Tablet, Film Coated · Oral
Product NDC72789-511
Product details
- Brand name
- Ciprofloxacin
- Generic name
- Ciprofloxacin Hydrochloride
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA077859
- Marketed since
- February 9, 2024
- Marketing end
- February 29, 2028
- Pharmacologic class
- Fluoroquinolone Antibacterial
Active ingredients
- Ciprofloxacin Hydrochloride 500 mg/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 72789-511-10 | 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-511-10) | Aug 27, 2025 |
| 72789-511-14 | 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-511-14) | Jul 31, 2025 |
| 72789-511-20 | 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-511-20) | Sep 12, 2025 |
| 72789-511-30 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-511-30) | Jun 2, 2025 |
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