NDC 67296-2135 – Ciprofloxacin
Ciprofloxacin Hydrochloride 500 mg/1 · Tablet · Oral
Product NDC67296-2135
Product details
- Brand name
- Ciprofloxacin
- Generic name
- Ciprofolxacin
- Labeler
- Redpharm Drug
- 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 (4)
| Package NDC | Description | Since |
|---|---|---|
| 67296-2135-1 | 14 TABLET in 1 BOTTLE (67296-2135-1) | Oct 1, 2023 |
| 67296-2135-2 | 10 TABLET in 1 BOTTLE (67296-2135-2) | Oct 1, 2023 |
| 67296-2135-3 | 20 TABLET in 1 BOTTLE (67296-2135-3) | Oct 1, 2023 |
| 67296-2135-6 | 6 TABLET in 1 BOTTLE (67296-2135-6) | Oct 1, 2023 |
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