NDC 51655-216 – Ciprofloxacin
Ciprofloxacin Hydrochloride 500 mg/1 · Tablet, Film Coated · Oral
Product NDC51655-216
Product details
- Brand name
- Ciprofloxacin
- Generic name
- Ciprofloxacin Hydrochloride
- Labeler
- Northwind Health Company, LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA077859
- Marketed since
- March 17, 2023
- Marketing end
- February 28, 2027
- Pharmacologic class
- Fluoroquinolone Antibacterial
Active ingredients
- Ciprofloxacin Hydrochloride 500 mg/1
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 51655-216-20 | 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-216-20) | Jun 28, 2023 |
| 51655-216-25 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-216-25) | Aug 18, 2023 |
| 51655-216-52 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-216-52) | Jan 10, 2024 |
| 51655-216-53 | 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-216-53) | Jul 14, 2023 |
| 51655-216-84 | 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-216-84) | Jun 8, 2023 |
| 51655-216-87 | 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-216-87) | Mar 17, 2023 |
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