NDC 68071-3737 – Ciprofloxacin
Ciprofloxacin Hydrochloride 500 mg/1 · Tablet · Oral
Product NDC68071-3737
Product details
- Brand name
- Ciprofloxacin
- Generic name
- Ciprofolxacin
- Labeler
- NuCare Pharmaceutical, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA208921
- Marketed since
- October 1, 2023
- Listing expires
- December 31, 2027
- Pharmacologic class
- Fluoroquinolone Antibacterial
Active ingredients
- Ciprofloxacin Hydrochloride 500 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 68071-3737-2 | 2 TABLET in 1 BOTTLE (68071-3737-2) | Dec 5, 2024 |
| 68071-3737-4 | 4 TABLET in 1 BOTTLE (68071-3737-4) | Aug 21, 2026 |
| 68071-3737-6 | 6 TABLET in 1 BOTTLE (68071-3737-6) | Jun 4, 2025 |
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