NDC 76420-929 – Ciprofloxacin
Ciprofloxacin Hydrochloride 500 mg/1 · Tablet · Oral
Product NDC76420-929
Product details
- Brand name
- Ciprofloxacin
- Generic name
- Ciprofolxacin
- Labeler
- Asclemed USA, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA208921
- Marketed since
- October 1, 2023
- Listing expires
- December 31, 2027
- Pharmacologic class
- Fluoroquinolone Antibacterial
Active ingredients
- Ciprofloxacin Hydrochloride 500 mg/1
Package NDC codes (7)
| Package NDC | Description | Since |
|---|---|---|
| 76420-929-01 | 100 TABLET in 1 BOTTLE (76420-929-01) | Mar 28, 2025 |
| 76420-929-05 | 500 TABLET in 1 BOTTLE (76420-929-05) | Mar 28, 2025 |
| 76420-929-14 | 14 TABLET in 1 BOTTLE (76420-929-14) | Jun 27, 2026 |
| 76420-929-20 | 20 TABLET in 1 BOTTLE (76420-929-20) | Mar 28, 2025 |
| 76420-929-30 | 30 TABLET in 1 BOTTLE (76420-929-30) | Mar 28, 2025 |
| 76420-929-60 | 60 TABLET in 1 BOTTLE (76420-929-60) | Mar 28, 2025 |
| 76420-929-90 | 90 TABLET in 1 BOTTLE (76420-929-90) | Mar 28, 2025 |
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