NDC 68788-8136 – Ciprofloxacin
Ciprofloxacin Hydrochloride 500 mg/1 · Tablet, Film Coated · Oral
Product NDC68788-8136
Product details
- Brand name
- Ciprofloxacin
- Generic name
- Ciprofloxacin Hydrochloride
- Labeler
- Preferred Pharmaceuticals Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA077859
- Marketed since
- February 3, 2022
- Listing expires
- December 31, 2026
- Pharmacologic class
- Fluoroquinolone Antibacterial
Active ingredients
- Ciprofloxacin Hydrochloride 500 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 68788-8136-0 | 6 TABLET, FILM COATED in 1 BOTTLE (68788-8136-0) | Feb 3, 2022 |
| 68788-8136-1 | 14 TABLET, FILM COATED in 1 BOTTLE (68788-8136-1) | Feb 3, 2022 |
| 68788-8136-2 | 20 TABLET, FILM COATED in 1 BOTTLE (68788-8136-2) | Feb 3, 2022 |
| 68788-8136-3 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-8136-3) | Feb 3, 2022 |
| 68788-8136-8 | 10 TABLET, FILM COATED in 1 BOTTLE (68788-8136-8) | Feb 3, 2022 |
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