NDC 72189-623 – Ciprofloxacin
Ciprofloxacin Hydrochloride 500 mg/1 · Tablet · Oral
Product NDC72189-623
Product details
- Brand name
- Ciprofloxacin
- Generic name
- Ciprofloxacin
- Labeler
- Direct_Rx
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA208921
- Marketed since
- May 14, 2025
- Listing expires
- December 31, 2027
- Pharmacologic class
- Fluoroquinolone Antibacterial
Active ingredients
- Ciprofloxacin Hydrochloride 500 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 72189-623-10 | 10 TABLET in 1 BOTTLE (72189-623-10) | May 14, 2025 |
| 72189-623-14 | 14 TABLET in 1 BOTTLE (72189-623-14) | May 14, 2025 |
| 72189-623-20 | 20 TABLET in 1 BOTTLE (72189-623-20) | May 14, 2025 |
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