NDC 70518-4214 – Ciprofloxacin
Ciprofloxacin Hydrochloride 500 mg/1 · Tablet, Film Coated · Oral
Product NDC70518-4214
Product details
- Brand name
- Ciprofloxacin
- Generic name
- Ciprofloxacin Hydrochloride
- Labeler
- REMEDYREPACK INC.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA077859
- Marketed since
- October 15, 2024
- Marketing end
- February 29, 2028
- Pharmacologic class
- Fluoroquinolone Antibacterial
Active ingredients
- Ciprofloxacin Hydrochloride 500 mg/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 70518-4214-0 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4214-0) | Oct 15, 2024 |
| 70518-4214-1 | 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4214-1) | Oct 25, 2024 |
| 70518-4214-2 | 14 TABLET, FILM COATED in 1 BLISTER PACK (70518-4214-2) | Nov 13, 2024 |
| 70518-4214-3 | 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4214-3) | May 12, 2026 |
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