NDC 70518-4229 – Ciprofloxacin
Ciprofloxacin Hydrochloride 500 mg/1 · Tablet · Oral
Product NDC70518-4229
Product details
- Brand name
- Ciprofloxacin
- Generic name
- Ciprofolxacin
- Labeler
- REMEDYREPACK INC.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA208921
- Marketed since
- November 11, 2024
- Listing expires
- December 31, 2027
- Pharmacologic class
- Fluoroquinolone Antibacterial
Active ingredients
- Ciprofloxacin Hydrochloride 500 mg/1
Package NDC codes (9)
| Package NDC | Description | Since |
|---|---|---|
| 70518-4229-0 | 14 TABLET in 1 BOTTLE, PLASTIC (70518-4229-0) | Nov 11, 2024 |
| 70518-4229-1 | 20 TABLET in 1 BLISTER PACK (70518-4229-1) | Dec 11, 2024 |
| 70518-4229-2 | 20 TABLET in 1 BOTTLE, PLASTIC (70518-4229-2) | Jan 14, 2025 |
| 70518-4229-3 | 30 TABLET in 1 BLISTER PACK (70518-4229-3) | Jan 29, 2025 |
| 70518-4229-4 | 14 TABLET in 1 BLISTER PACK (70518-4229-4) | May 19, 2025 |
| 70518-4229-5 | 14 TABLET in 1 BOTTLE, PLASTIC (70518-4229-5) | Jul 9, 2025 |
| 70518-4229-6 | 30 TABLET in 1 BLISTER PACK (70518-4229-6) | Jul 31, 2025 |
| 70518-4229-7 | 30 TABLET in 1 BOTTLE, PLASTIC (70518-4229-7) | Jan 26, 2026 |
| 70518-4229-8 | 10 TABLET in 1 BOTTLE, PLASTIC (70518-4229-8) | Jul 28, 2026 |
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