NDC 68071-3610 – Ciprofloxacin
Ciprofloxacin Hydrochloride 500 mg/1 · Tablet · Oral
Product NDC68071-3610
Product details
- Brand name
- Ciprofloxacin
- Generic name
- Ciprofolxacin
- Labeler
- NuCare 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 500 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 68071-3610-1 | 10 TABLET in 1 BOTTLE (68071-3610-1) | Jun 17, 2024 |
| 68071-3610-2 | 20 TABLET in 1 BOTTLE (68071-3610-2) | Jun 17, 2024 |
| 68071-3610-4 | 14 TABLET in 1 BOTTLE (68071-3610-4) | Jun 17, 2024 |
| 68071-3610-6 | 6 TABLET in 1 BOTTLE (68071-3610-6) | Aug 5, 2025 |
| 68071-3610-8 | 28 TABLET in 1 BOTTLE (68071-3610-8) | Dec 3, 2025 |
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