NDC 68071-4260 – ciprofloxacin
Ciprofloxacin Hydrochloride 250 mg/1 · Tablet · Oral
Product NDC68071-4260
Product details
- Brand name
- ciprofloxacin
- Generic name
- ciprofloxacin
- Labeler
- NuCare Pharmaceuticals,Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA076639
- Marketed since
- September 10, 2004
- Listing expires
- December 31, 2026
- Pharmacologic class
- Fluoroquinolone Antibacterial
Active ingredients
- Ciprofloxacin Hydrochloride 250 mg/1
Package NDC codes (8)
| Package NDC | Description | Since |
|---|---|---|
| 68071-4260-2 | 21 TABLET in 1 BOTTLE (68071-4260-2) | Jan 31, 2018 |
| 68071-4260-3 | 30 TABLET in 1 BOTTLE (68071-4260-3) | Jan 31, 2018 |
| 68071-4260-4 | 14 TABLET in 1 BOTTLE (68071-4260-4) | Jan 31, 2018 |
| 68071-4260-5 | 20 TABLET in 1 BOTTLE (68071-4260-5) | Jan 31, 2018 |
| 68071-4260-6 | 6 TABLET in 1 BOTTLE (68071-4260-6) | Jan 31, 2018 |
| 68071-4260-7 | 10 TABLET in 1 BOTTLE (68071-4260-7) | Jan 31, 2018 |
| 68071-4260-8 | 28 TABLET in 1 BOTTLE (68071-4260-8) | Jan 31, 2018 |
| 68071-4260-9 | 90 TABLET in 1 BOTTLE (68071-4260-9) | Jan 31, 2018 |
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