NDC 72789-519 – Ciprofloxacin
Ciprofloxacin Hydrochloride 250 mg/1 · Tablet · Oral
Product NDC72789-519
Product details
- Brand name
- Ciprofloxacin
- Generic name
- Ciprofolxacin
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA208921
- Marketed since
- October 1, 2023
- Listing expires
- December 31, 2026
- Pharmacologic class
- Fluoroquinolone Antibacterial
Active ingredients
- Ciprofloxacin Hydrochloride 250 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 72789-519-06 | 6 TABLET in 1 BOTTLE, PLASTIC (72789-519-06) | Sep 18, 2025 |
| 72789-519-10 | 10 TABLET in 1 BOTTLE, PLASTIC (72789-519-10) | Aug 22, 2025 |
| 72789-519-12 | 12 TABLET in 1 BOTTLE, PLASTIC (72789-519-12) | Oct 24, 2025 |
| 72789-519-14 | 14 TABLET in 1 BOTTLE, PLASTIC (72789-519-14) | Jul 31, 2025 |
| 72789-519-20 | 20 TABLET in 1 BOTTLE, PLASTIC (72789-519-20) | Sep 10, 2025 |
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