NDC 68071-4122 – ciprofloxacin
Ciprofloxacin Hydrochloride 500 mg/1 · Tablet · Oral
Product NDC68071-4122
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 500 mg/1
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 68071-4122-1 | 10 TABLET in 1 BOTTLE (68071-4122-1) | Oct 16, 2017 |
| 68071-4122-2 | 20 TABLET in 1 BOTTLE (68071-4122-2) | Oct 16, 2017 |
| 68071-4122-3 | 30 TABLET in 1 BOTTLE (68071-4122-3) | Oct 16, 2017 |
| 68071-4122-4 | 14 TABLET in 1 BOTTLE (68071-4122-4) | Oct 16, 2017 |
| 68071-4122-6 | 60 TABLET in 1 BOTTLE (68071-4122-6) | Oct 16, 2017 |
| 68071-4122-7 | 21 TABLET in 1 BOTTLE (68071-4122-7) | Oct 16, 2017 |
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