NDC 68788-8692 – Ciprofloxacin
Ciprofloxacin Hydrochloride 500 mg/1 · Tablet · Oral
Product NDC68788-8692
Product details
- Brand name
- Ciprofloxacin
- Generic name
- Ciprofolxacin
- Labeler
- Preferred Pharmaceuticals Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA208921
- Marketed since
- June 10, 2024
- Listing expires
- December 31, 2027
- Pharmacologic class
- Fluoroquinolone Antibacterial
Active ingredients
- Ciprofloxacin Hydrochloride 500 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 68788-8692-0 | 6 TABLET in 1 BOTTLE (68788-8692-0) | Jun 10, 2024 |
| 68788-8692-1 | 14 TABLET in 1 BOTTLE (68788-8692-1) | Jun 10, 2024 |
| 68788-8692-2 | 20 TABLET in 1 BOTTLE (68788-8692-2) | Jun 10, 2024 |
| 68788-8692-3 | 30 TABLET in 1 BOTTLE (68788-8692-3) | Jun 10, 2024 |
| 68788-8692-8 | 10 TABLET in 1 BOTTLE (68788-8692-8) | Jun 10, 2024 |
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